262295-96-5

Basic information

• Product Name: 3-Pyridinemethanamine,6-methoxy-(9CI)
• Synonyms: 3-Pyridinemethanamine,6-methoxy-(9CI);5-(AMinoMethyl)-2-Methoxypyridine;6-Methoxy-3-PyridineMethanaMine;3-PyridineMethanaMine, 6-Methoxy-;(6-Methoxypyridin-3-yl)methylamine, 6-Methoxynicotinylamine;5-AMinoMethyl-2-Methoxypyridine hydrochloride;3-Aminomethyl-6-methoxypyridine;6-Methoxypyridine-3-methanamine
• CAS NO: 262295-96-5
• Molecular Formula: C₇H₁₀N₂O
• Molecular Weight: 138.169
• Product Categories: PYRIDINE
• Mol File: 262295-96-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 239.342ºC at 760 mmHg
• Flash Point: 98.551ºC
• Appearance: /
• Density: 1.091g/cm3
• Vapor Pressure: 0.04mmHg at 25°C
• Refractive Index: 1.536
• Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
• PKA: 7.94±0.29(Predicted)
• CAS DataBase Reference: 3-Pyridinemethanamine,6-methoxy-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinemethanamine,6-methoxy-(9CI)(262295-96-5)
• EPA Substance Registry System: 3-Pyridinemethanamine,6-methoxy-(9CI)(262295-96-5)

Safety Data

• RIDADR: 3265
• HazardClass: 8
• PackingGroup: Ⅲ
• Hazardous Substances Data: 262295-96-5(Hazardous Substances Data)

Usage

Application

5-(Aminomethyl)-2-methoxypyridine is a useful research chemical for organic synthesis and other chemical processes.

InChI:InChI=1/C7H10N2O/c1-10-7-3-2-6(4-8)5-9-7/h2-3,5H,4,8H2,1H3

Upstream product

• 1178036-30-0 2-{[(6-methoxypyridin-3-yl)methyl]carbamoyl}benzoic acid 
• 13473-01-3 5-chloro-2-methoxypyridine 
• 6271-78-9 6-chloro-3-pyridinecarboxamide 
• 5006-66-6 6-hydroxy-3-pyridinecarboxylic acid 
• 33252-28-7 6-chloronicotinonitrile 
• 124-41-4 sodium methylate 
• 97004-04-1 5-(aminomethyl)-2-chloropyridine 
• 15871-85-9 6-methoxynicotinonitrile 

Downstream Products

• 1439358-00-5 C₂₀H₁₉N₃O₄S 
• 1429939-75-2 C₂₂H₂₂F₃N₅O₂ 
• 1421455-10-8 C₂₃H₂₀F₃N₅O₄ 
• 1421454-82-1 C₂₃H₂₃N₅O₄ 

Relevant articles and documents

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The catalytic transfer hydrogenation of (hetero)aryl nitriles using ammonium formate has been investigated in detail. In the presence of commercially available Pd/C, a straightforward and selective reduction is achieved without any additives under mild conditions.

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7-Substituted Purine Derivatives for Immunosuppression

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