Month: October 2022

Pyridine is diamagnetic and has a diamagnetic susceptibility of −48.7 × 10−6 cm3·mol−1.The molecular electric dipole moment is 2.2 debyes. 16133-25-8, formula is C5H4ClNO2S, Name is Pyridine-3-sulfonyl chloride. TThe standard enthalpy of formation is 100.2 kJ·mol−1 in the liquid phase and 140.4 kJ·mol−1 in the gas phase. Application In Synthesis of 16133-25-8.

White, Dawn H.;Noble, Adam;Booker-Milburn, Kevin I.;Aggarwal, Varinder K. research published 《 Diastereoselective Photoredox-Catalyzed [3 + 2] Cycloadditions of N-Sulfonyl Cyclopropylamines with Electron-Deficient Olefins》, the research content is summarized as follows. A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopropylamines I (R = Ph, 4-MeC₆H₄, 2-naphthyl, 3-pyridinyl, etc.) and electron-deficient olefins R¹R²C:CHR³ (R¹ = EtO₂C, CN, PhCO, PhNHCO, etc., R² = H, Me, R³ = H; R¹ = R² = EtO₂C, R³ = Me; R¹ = Ph, R² = H, R³ = MeO₂C; etc.) is reported. The reactions proceed via the oxidation of a sulfonamide aza-anion by an organic photocatalyst to generate a nitrogen-centered radical. Strain-induced ring opening and intermol. addition to the olefin generate an intermediate carbon-centered radical that is reduced to an anion prior to 5-exo cyclization. This enables a highly diastereoselective construction of trans-cyclopentanes II possessing synthetically useful functional groups.

16133-25-8, Pyridine-3-sulfonyl chloride is a useful research compound. Its molecular formula is C5H4ClNO2S and its molecular weight is 177.61 g/mol. The purity is usually 95%.
Pyridine-3-sulfonyl chloride is a reagent used in the synthesis of pyrimidine derivatives with anti-proliferative activity against negative breast cancer cells.
Pyridine-3-sulfonyl chloride is a chemical compound that binds to the active site of cytochrome P450 enzymes. It can be used to study the effects of matrix effect on reaction solution. Pyridine-3-sulfonyl chloride has been shown to have an UV absorption spectrum with a maximum at 280 nm and a p450 activity that is proportional to the concentration of human serum. This compound has been shown to inhibit kinase domain in vitro assays, which may have clinical relevance in the treatment of obesity., Application In Synthesis of 16133-25-8

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

At 25 °C pyridine has a viscosity of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1. 766-11-0, formula is C5H3BrFN, Name is 5-Bromo-2-fluoropyridine. The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point. Reference of 766-11-0.

White, Catherine;McGowan, Meredeth A.;Zhou, Hua;Sciammetta, Nunzio;Fradera, Xavier;Lim, Jongwon;Joshi, Elizabeth M.;Andrews, Christine;Nickbarg, Elliott B.;Cowley, Phillip;Trewick, Sarah;Augustin, Martin;von Koenig, Konstanze;Lesburg, Charles A.;Otte, Karin;Knemeyer, Ian;Woo, Hyun;Yu, Wensheng;Cheng, Mangeng;Spacciapoli, Peter;Geda, Prasanthi;Song, Xuelei;Smotrov, Nadya;Curran, Patrick;Heo, Mee Ra;Abeywickrema, Pravien;Miller, J. Richard;Bennett, David Jonathan;Han, Yongxin research published 《 Strategic Incorporation of Polarity in Heme-Displacing Inhibitors of Indoleamine-2,3-dioxygenase-1 (IDO1)》, the research content is summarized as follows. Indoleamine-2,3-dioxygenase-1 (IDO1) has emerged as a target of significant interest to the field of cancer immunotherapy, as the upregulation of IDO1 in certain cancers has been linked to host immune evasion and poor prognosis for patients. In particular, IDO1 inhibition is of interest as a combination therapy with immune checkpoint inhibition. Through an Automated Ligand Identification System (ALIS) screen, a diamide class of compounds was identified as a promising lead for the inhibition of IDO1. While hit 1() possessed attractive cell-based potency, it suffered from a significant right-shift in a whole blood assay, poor solubility, and poor pharmacokinetic properties. Through a physicochem. property-based approach, including a focus on lowering AlogP₉₈ via the strategic introduction of polar substitution, compound 13 was identified bearing a pyridyl oxetane core. Compound 13() demonstrated improved whole blood potency and solubility, and an improved pharmacokinetic profile resulting in a low predicted human dose.

766-11-0, 5-Bromo-2-fluoropyridine is a useful research compound. Its molecular formula is C5H3BrFN and its molecular weight is 175.99 g/mol. The purity is usually 95%.
5-Bromo-2-fluoropyridine is a boronic acid that has been shown to react with iodides and form 5-bromo-2-fluoroiodobenzene. The reaction of 5-bromo-2-fluoropyridine with benzene gives the same product as the reaction with 1,3,5-trioxane. The UV absorption of 5-bromo-2-fluoropyridine is found at 230 nm and 260 nm. It also has an absorption band in the infrared region at 1625 cm−1. Vibrational progressions have been observed for this molecule, which are due to dipole moments and electron density distributions in the molecule.
5-bromo-2-fluoropyridine is used in the synthesis of heteroaromatic and aniline derivatives of piperidines as potent ligands used for vesicular acetylcholine transport. , Reference of 766-11-0

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is diamagnetic and has a diamagnetic susceptibility of −48.7 × 10−6 cm3·mol−1.The molecular electric dipole moment is 2.2 debyes. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. TThe standard enthalpy of formation is 100.2 kJ·mol−1 in the liquid phase and 140.4 kJ·mol−1 in the gas phase. Recommanded Product: 2-Amino-5-methylpyridine.

Weiss, Alexander K. H.;Wurzer, Richard;Klapec, Patrycia;Eder, Manuel Philip;Loeffler, Johannes R.;von Grafenstein, Susanne;Monteleone, Stefania;Liedl, Klaus R.;Jansen-Duerr, Pidder;Gstach, Hubert research published 《 Inhibitors of Fumarylacetoacetate Hydrolase Domain Containing Protein 1 (FAHD1)》, the research content is summarized as follows. FAH domain containing protein 1 (FAHD1) acts as oxaloacetate decarboxylase in mitochondria, contributing to the regulation of the tricarboxylic acid cycle. Guided by a high-resolution X-ray structure of FAHD1 liganded by oxalate, the enzymic mechanism of substrate processing is analyzed in detail. Taking the chem. features of the FAHD1 substrate oxaloacetate into account, the potential inhibitor structures are deduced. The synthesis of drug-like scaffolds afforded first-generation FAHD1-inhibitors with activities in the low micromolar IC₅₀ range. The investigations disclosed structures competing with the substrate for binding to the metal cofactor, as well as scaffolds, which may have a novel binding mode to FAHD1.

Recommanded Product: 2-Amino-5-methylpyridine, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, 1603-41-4.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is diamagnetic and has a diamagnetic susceptibility of −48.7 × 10−6 cm3·mol−1.The molecular electric dipole moment is 2.2 debyes. 16133-25-8, formula is C5H4ClNO2S, Name is Pyridine-3-sulfonyl chloride. TThe standard enthalpy of formation is 100.2 kJ·mol−1 in the liquid phase and 140.4 kJ·mol−1 in the gas phase. Synthetic Route of 16133-25-8.

Wei, Jingjing;Liang, Shuaishuai;Jiang, Lvqi;Mumtaz, Yasir;Yi, Wen-bin research published 《 Regioselective Chloro-thiolation of Alkenes with Sulfonyl Chlorides》, the research content is summarized as follows. A newly developed sulfonyl chlorides-based regioselective chloro-thiolation of alkenes has been disclosed, the reaction is compatible with a variety of functional groups and can be scaled up to the gram-scale with no loss in yield. The employment of readily available reactants, mild reaction conditions, and high regioselectivity makes this process very practical. Mechanistic studies revealed a possible free radical reaction pathway.

Synthetic Route of 16133-25-8, Pyridine-3-sulfonyl chloride is a useful research compound. Its molecular formula is C5H4ClNO2S and its molecular weight is 177.61 g/mol. The purity is usually 95%.
Pyridine-3-sulfonyl chloride is a reagent used in the synthesis of pyrimidine derivatives with anti-proliferative activity against negative breast cancer cells.
Pyridine-3-sulfonyl chloride is a chemical compound that binds to the active site of cytochrome P450 enzymes. It can be used to study the effects of matrix effect on reaction solution. Pyridine-3-sulfonyl chloride has been shown to have an UV absorption spectrum with a maximum at 280 nm and a p450 activity that is proportional to the concentration of human serum. This compound has been shown to inhibit kinase domain in vitro assays, which may have clinical relevance in the treatment of obesity., 16133-25-8.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is colorless, but older or impure samples can appear yellow. 5315-25-3, formula is C6H6BrN, Name is 2-Bromo-6-methylpyridine. The pyridine ring occurs in many important compounds, including agrochemicals, pharmaceuticals, and vitamins. Historically, pyridine was produced from coal tar. Product Details of C6H6BrN.

Waters, Jessica E.;Hanf, Schirin;Rincon-Nocito, Marina;Bond, Andrew D.;Garcia-Rodriguez, Raul;Wright, Dominic S.;Colebatch, Annie L. research published 《 Synthesis and coordination behavior of aluminate-based quinolyl ligands》, the research content is summarized as follows. Lithium tris-quinolinylaluminate complexes were prepared by transmetalation of quinolinyllithium compounds with EtAlCl₂; the electronic and steric effects of substitution of 2-quinolinyl groups for remote 8-quinolinyl groups were evaluated by single-crystal x-ray diffraction anal. and theor. calculations The effects of moving the donor N-atom from the 2-position in lithium (2-pyridyl)- and (2-quinolyl)aluminates to the more remote position in (8-quinolyl)aluminates have been investigated by solid-state structural and DFT computational studies of the new complexes [{EtAl(2-qy)₃}Li(μ-X)Li(THF)₃] (X = Cl/Br 62:38) [(1)Li(μ-X)Li(THF)₃], [{(EtAl(2-qy)₃)Li}₂(μ-Br)]^–Li(THF)₄⁺ [{1Li}₂(μ-Br)]^–Li(THF)₄⁺, [{EtAl(2-Me-8-qy)₃}Li] [(2)Li], [{Me₂Al(2-Me-8-qy)₂}Li(THF)] [(3a)Li(THF)], [{Me₂Al(6-Me-2-py)₂}Li(THF)₂] [(4)Li(THF)₂] and [{{EtAl(2-Me-8-qy)₂}₂O}(Li₂THF)] (5). Increasing the remoteness of the donor N-atom from the bridgehead results in large differences in the coordination of the Li⁺ cations by the (8-quinolyl)aluminate anions compared to 2-quinolyl or 2-pyridyl counterparts. The results are of potential interest in understanding how the coordination sites of ligands of this type can be tuned for the coordination requirements of specific metal centers.

5315-25-3, 2-Bromo-6-methylpyridine (2BMPy) is a bromopyridine derivative. It is formed when 2-chloro-6-methylpyridine is heated with bromotrimethylsilane. Its synthesis from various methods have been reported.
2-Bromo-6-methylpyridine is a building block in the preparation of nitrogen containing heterocyclic compounds.
2-Bromo-6-methylpyridine is an organic compound that belongs to the group of pyridinium halides. It is soluble in common solvents such as water, ethanol, and acetone. 2BMPy has been shown to act as a glutamate receptor antagonist and has been used in the study of glutamate receptors, including their subtypes. This chemical has also been shown to have antioxidant properties and can be used in the prevention of atherosclerosis., Product Details of C6H6BrN

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine has a conjugated system of six π electrons that are delocalized over the ring. 31181-90-5, formula is C6H4BrNO, Name is 5-Bromopicolinaldehyde. The molecule is planar and, thus, follows the Hückel criteria for aromatic systems. HPLC of Formula: 31181-90-5.

Wang, Zihua;Zheng, Chunhong;Xu, Dongming;Liao, Guanming;Pu, Shouzhi research published 《 A fluorescent sensor for Zn²⁺ and Cd²⁺ based on a diarylethene derivative with an indole-2-methylhydrazone moiety》, the research content is summarized as follows. A fluorescent sensor for Zn²⁺ and Cd²⁺ based on a diarylethene derivative with an indole-2-methylhydrazone moiety was constructed. The photochromism and photoswitchable fluorescence can be reversibly modulated by UV/Vis light and M²⁺/EDTA (M = Zn²⁺ or Cd2+). Upon addition of Zn²⁺ or Cd²⁺, an obviously large red-shift emission peak by 105 nm, and fluorescence quantum yields enhanced by 72-fold and 48-fold, resp., with a concomitant black-to-green fluorescence color change was observed The 1:1 stoichiometry complexes with Zn²⁺ and Cd²⁺ were confirmed by both Job′s plot and Benesi-Hildebrand expression. As a result, the binding constants between sensor and metal ions were calculated to be 8.88 x 10⁴ L mol^-1 for Zn²⁺ and 4.36 x 10⁴ L mol^-1 for Cd²⁺, resp. And the detection limit of 1o for Zn²⁺ and Cd²⁺ was 3.82 x 10^-7 mol L^-1, and 5.74 x 10^-7 mol L^-1, resp. Moreover, the fluorescent can be used to detect Zn²⁺ and Cd²⁺ in tap water sample with a high accuracy.

31181-90-5, 5-Bromopyridine-2-carbaldehyde is a useful research compound. Its molecular formula is C6H4BrNO and its molecular weight is 186.01 g/mol. The purity is usually 95%.

5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%., HPLC of Formula: 31181-90-5

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. Reference of 1603-41-4.

Wang, Yuhan;Zheng, Huitao;Xu, Jiajia;Zhuang, Canzhan;Liu, Xiang;Cao, Hua research published 《 Access to diverse primary, secondary, and tertiary amines via the merger of controllable cleavage of triazines and site-selective functionalization》, the research content is summarized as follows. An efficient approach for divergent synthesis of primary, secondary, and tertiary amines, e.g., I via the merger of controllable cleavage of triazines and site-selective functionalization was disclosed. This transformation proceeded with imidazo[1,2-a]pyridines and readily available triazines by Lewis acid catalysis and Hofmann-Martius type rearrangement. A number of imidazo [1,2-a]pyridines-containing primary and secondary aromatic amines, and trialkylamines were facilely accessed with a wide range of functional groups. Importantly, the obtained aromatic amines could be incorporated with important bioactive units and converted into many valuable nitrogen-containing mols. In addition, the results revealed that Hofmann-Martius type rearrangement exhibits excellent o- and p-selectivity and goes through an intermol. process.

1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, Reference of 1603-41-4

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

At 25 °C pyridine has a viscosity of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1. 31181-90-5, formula is C6H4BrNO, Name is 5-Bromopicolinaldehyde. The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point. Quality Control of 31181-90-5.

Wang, Yuesong;Yu, Haoli;Chen, Yan;Cui, Mengyuan;Ji, Min research published 《 Synthesis and application of near-infrared dyes based on sulfur-substituted dicyanomethylene-4H-chromene and diarylethene》, the research content is summarized as follows. Four novel compounds (S-DCM-1O, S-DCM-2O, S-DCM-3O, and S-DCM-4O) based on sulfur-substituted dicyanomethylene-4H-chromene (S-DCM) and diarylethene were synthesized. The detailed investigations on the fluorescence spectra, absorption spectra, and time-dependent d. functional theory calculations (DFT/TD-DFT) were presented. The encapsulation of mPEG2000-DSPE effectively increased the solubility of all the as-prepared samples. The results of TEM showed that the nanoparticles had a good dispersion coefficient All the nanomaterials (S-DCM-1O@PEG, S-DCM-2O@PEG, S-DCM-3O@PEG, and S-DCM-4O@PEG) exhibited near-IR emission (650-900 nm) and thus reduced light damage and light scattering for cell imaging in biol. applications. Furthermore, PLL (poly-L-lysine hydrobromide) was used to modify the surface of nanoparticles to facilitate easy uptake by A549 cells by changing their electronegativity. The results suggested that S-DCM-2O@PEG@PLL was a highly suitable candidate for cell imaging because of its low toxicity and excellent biocompatibility.

31181-90-5, 5-Bromopyridine-2-carbaldehyde is a useful research compound. Its molecular formula is C6H4BrNO and its molecular weight is 186.01 g/mol. The purity is usually 95%.

5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%., Quality Control of 31181-90-5

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

At 25 °C pyridine has a viscosity of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point. Application In Synthesis of 1603-41-4.

Wang, Yishou;Li, Shichen;Wang, Xinfeng;Yao, Yiming;Feng, Lei;Ma, Chen research published 《 A multi pathway coupled domino strategy: I₂/TBHP-promoted synthesis of imidazopyridines and thiazoles via sp³, sp² and sp C-H functionalization》, the research content is summarized as follows. I₂/TBHP-promoted, one-pot, multi pathway synthesis of imidazopyridines and thiazoles was achieved through readily available ethylarenes, ethylenearenes and ethynearenes. I₂/TBHP as an initiator and oxidant was used to realize the C-H functionalization of this domino reaction. Simple and available starting materials, wide range of functional group tolerance, high potential for drug activity of the products and application in production were the advantageous features of this method.

1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, Application In Synthesis of 1603-41-4

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. 5315-25-3, formula is C6H6BrN, Name is 2-Bromo-6-methylpyridine. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. Computed Properties of 5315-25-3.

Wang, Yi-Dong;Liu, Jin-Kui;Yang, Xue-Jie;Gong, Jun-Fang;Song, Mao-Ping research published 《 Chiral (Pyridine)-(Imidazoline) NCN’ Pincer Palladium(II) Complexes: Convenient Synthesis via C-H Activation and Characterization》, the research content is summarized as follows. A series of aryl-based chiral NCN’ pincer palladium(II) complexes 4a–k were synthesized via C-H activation of the (pyridyl)-(imidazolinyl)benzene ligands, which proceeded smoothly with PdCl₂ as the palladium source in the presence of Et₃N or NaHCO₃ base in toluene under reflux. All of the complexes have been characterized by elemental anal. and ¹H and ¹³C{¹H} NMR spectroscopy. In addition, the mol. structures of complexes 4a, 4c, and 4f have been determined by x-ray single-crystal diffraction anal. The obtained chiral Pd pincers were applied to catalytic asym. reactions of acrylonitrile and dichloroacetonitrile with sulfonimines. With a catalyst loading of 5 mol % and the assistance of AgOAc, these complexes acted as active but moderately stereoselective catalysts for the aforementioned reactions.

5315-25-3, 2-Bromo-6-methylpyridine (2BMPy) is a bromopyridine derivative. It is formed when 2-chloro-6-methylpyridine is heated with bromotrimethylsilane. Its synthesis from various methods have been reported.
2-Bromo-6-methylpyridine is a building block in the preparation of nitrogen containing heterocyclic compounds.
2-Bromo-6-methylpyridine is an organic compound that belongs to the group of pyridinium halides. It is soluble in common solvents such as water, ethanol, and acetone. 2BMPy has been shown to act as a glutamate receptor antagonist and has been used in the study of glutamate receptors, including their subtypes. This chemical has also been shown to have antioxidant properties and can be used in the prevention of atherosclerosis., Computed Properties of 5315-25-3

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem