23974-15-4

Basic information

• Product Name: 4-Acetylaminomethyl pyridine
• Synonyms: 4-Acetylaminomethyl pyridine
• CAS NO: 23974-15-4
• Molecular Formula: C₈H₁₀N₂O
• Molecular Weight: 150.1778
• Mol File: 23974-15-4.mol
• Article Data: 11

Chemical Properties

• Melting Point: 68-70 °C
• Boiling Point: 379.2°C at 760 mmHg
• Flash Point: 183.1°C
• Appearance: /
• Density: 1.088g/cm³
• Vapor Pressure: 5.95E-06mmHg at 25°C
• Refractive Index: 1.523
• PKA: 15.01±0.46(Predicted)
• CAS DataBase Reference: 4-Acetylaminomethyl pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Acetylaminomethyl pyridine(23974-15-4)
• EPA Substance Registry System: 4-Acetylaminomethyl pyridine(23974-15-4)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 23974-15-4(Hazardous Substances Data)

Usage

General Description

4-Acetylaminomethyl pyridine, also known as AAMP, is a chemical compound with the molecular formula C8H10N2O. It is a derivative of pyridine and contains an acetylaminomethyl group. AAMP is used in the synthesis of various pharmaceuticals and agrochemicals, and as a intermediate for the production of other organic compounds. It is also utilized as a reagent and catalyst in organic chemistry reactions. AAMP is known for its strong odor and should be handled with caution due to its potential health hazards.

InChI:InChI=1/C8H10N2O/c1-7(11)10-6-8-2-4-9-5-3-8/h2-5H,6H2,1H3,(H,10,11)

Upstream product

• 3731-53-1 4-(aminomethyl)pyridine 
• 581-55-5 benzylidene 1,1-diacetate 
• 75-36-5 acetyl chloride 
• 1363906-80-2 1-acetyl-2,3,4,6,7,8-hexahydropyrrolo[1,2-a]pyrimidinium tetraphenylborate 
• 696-54-8 pyridine-4-aldoxime 
• 64-19-7 acetic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 153196-16-8 2-hydroxy-2,2-diphenyl-N-<<1,2,3,6-tetrahydro-1-(4-methoxybenzyl)-4-pyridyl>methyl>acetamide 
• 131839-63-9 N-(1-benzyl-1,2,3,6-tetrahydropyridin-4-yl)-methyl-2-cyclohexyl-2-hydroxy-2-phenylacetamide 
• 153196-03-3 2-hydroxy-2,2-diphenyl-N-<(1,2,3,6-tetrahydro-4-pyridyl)methyl>acetamide 
• 153196-02-2 N-<(1-carbobenzyloxy-1,2,3,6-tetrahydro-4-pyridyl)methyl>-2-hydroxy-2,2-diphenylacetamide 

Relevant articles and documents

Syntheses of methylpyridine and methylpyridine N-oxide decorated benzoxazine and naphthoxazine platforms

Simple, aqueous-based syntheses of methylpyridine and methylpyridine N-oxide decorated 3,4-dihydro-2H-naphthoxazine and 2,3-dihydro-1H-naphthoxazine monomers, as well as thermally promoted syntheses of 3,4-dihydro-2H-benzoxazine monomers and bisoxazine methylpyridine derivatives of substituted 1,5-, 2,6-, and 2,7-dihydroxynaphthalenes are described. The crystal structures of two derivatives are presented.

Construction of 1,2,4-Triazole Derivatives via Cyclocondensation of Alkylidene Dihydropyridines and Aryldiazonium Salts

Alkylidene dihydropyridines (anhydrobases) prepared via dearomatization of N-acylated 4-(aminomethyl)pyridines participate in [3 + 2] cyclocondensation reactions with aryldiazonium cations to afford substituted 1,2,4-triazolium salts or neutral 1,2,4-tria

Hidden signatures: New reagents for developing latent fingerprints

Aldehydes substituted with a quaternised pyridinium or quinolinium ring have been investigated for the development of latent fingerprints. Two routes were developed to a novel in situ formed azacyanine dye. This dye might form in the fingerprint where rea