609770-35-6

Basic information

• Product Name: 2-(azidomethyl)pyridine(SALTDATA: FREE)
• Synonyms: 2-(azidomethyl)pyridine(SALTDATA: FREE)
• CAS NO: 609770-35-6
• Molecular Formula: C₆H₆N₄
• Molecular Weight: 134.13864
• Mol File: 609770-35-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(azidomethyl)pyridine(SALTDATA: FREE)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(azidomethyl)pyridine(SALTDATA: FREE)(609770-35-6)
• EPA Substance Registry System: 2-(azidomethyl)pyridine(SALTDATA: FREE)(609770-35-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 609770-35-6(Hazardous Substances Data)

Usage

General Description

2-(azidomethyl)pyridine is a chemical compound commonly used in organic synthesis and chemical research. It is a pyridine derivative with an azido group attached to the methyl group, and it is often used as a precursor in the synthesis of various organic compounds. The azido group can undergo various chemical reactions, such as azide-alkyne cycloaddition, to form new carbon-carbon or carbon-nitrogen bonds. The compound may also have potential applications in medicinal chemistry and pharmaceutical research. However, it is important to handle this compound with caution, as azides are known to be potentially explosive and toxic. Overall, 2-(azidomethyl)pyridine is an important building block in organic chemistry with potential applications in various fields.

Upstream product

• 4377-33-7 2-chloromethylpyridine 

Downstream Products

• 1192206-01-1 2-{[4-phenyl-1H-1,2,3-triazol-1-yl]methyl}pyridine 
• 1224434-24-5 2-(4-methoxyphenyl)-N-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl)diazenecarboxamide 
• 1224434-25-6 2-(4-fluorophenyl)-N-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl)diazenecarboxamide 
• 1224434-26-7 2-(4-nitrophenyl)-N-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl)diazenecarboxamide 
• 1224434-20-1 2-phenyl-N-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl)diazenecarboxamide 
• 1224434-21-2 N-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl)-2-p-tolyldiazenecarboxamide 
• 1224434-22-3 2-(4-chlorophenyl)-N-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl)diazenecarboxamide 
• 1224434-23-4 N-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methyl)-2-(4-(trifluoromethyl)phenyl)diazenecarboxamide 
• 1234381-72-6 2-(4-{4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-naphthalen-1-yl}-[1,2,3]triazol-1-ylmethyl)-pyridine 
• 1227780-04-2 1-tert-butyl-3-(6-(3,5-dimethoxyphenyl)-2-((1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)methylamino)pyrido[2,3-d]pyrimidin-7-yl)urea 
• 1227780-11-1 1-tert-butyl-3-(6-(3,5-dimethoxyphenyl)-2-(3-(1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl)propylamino)pyrido[2,3-d]pyrimidin-7-yl)urea 
• 1227780-12-2 1-tert-butyl-3-(6-(3,5-dimethoxyphenyl)-2-(4-(1-((pyridine-2-yl-methyl)methyl)-1H-1,2,3-triazol-4-yl)butylamino)pyrido[2,3-d]pyrimidin-7-yl)urea 
• 100-70-9 2-Cyanopyridine 
• 1246847-68-6 2-[(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)methyl]pyridine 

Relevant articles and documents

Synthesis, characterization and low temperature self assembling of (η3-allyl)palladium complexes with 2-pyridyl-1,2,3-triazole bidentate ligands. Study of the catalytic activity in Suzuki-Miyaura reaction

The cationic complexes [Pd(η3-C3H 5)(2-((4-propyl-1H-1,2,3-triazol-1-yl)methyl)pyridine)](X) (2: X = BF4-, 3: X = ClO4-), and [Pd(η3-2-CH3-C3Hsu

Pyridine-phosphinimine ligand-accelerated Cu(I)-catalyzed azide-alkyne cycloaddition for preparation of 1-(pyridin-2-yl)-1,2,3-triazole derivatives

A series of phosphinimine ligands were designed and used in the Cu(i)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction of tetrazolo[1,5-a]pyridines and alkynes for the first time. By optimizing the reaction conditions, an efficient catalytic system (CuCl/2-PyCH 2NPtBu3) was developed to give 1-(pyridin-2-yl)-1,2,3-triazole derivatives in moderate to excellent yields (46-98%). This journal is the Partner Organisations 2014.

Synthesis of click-chelator via Cu(I)-catalyzed alkyne-azide cycloaddition

The click-ligands based on 1,2,3-triazole and pyridine unit has been synthesized via Cu(I)-catalyzed alkyne-azide cycloaddition from corresponding organic azides and terminal alkynes. The ligand structure was characterized by NMR, IR and elemental analysis as well as single crystal diffractions. The single crystal structure of the complexes from two different ligands coordinating to Cu(II) and Co(II) ions indicated that the N(2) atom in 1,2,3-triazole unit can act as an efficient donor to metals through the rational molecular design. Copyright