51667-66-4

Basic information

• Product Name: 2-(5-Methyl-1H-imidazol-4-yl)acetonitrile
• Synonyms: 2-(5-Methyl-1H-imidazol-4-yl)acetonitrile;(4-methyl-1H-imidazol-5-yl)acetonitrile;2-(4-methyl-1H-imidazol-5-yl)acetonitrile;2-(5-methyl-1H-imidazol-4-yl)ethanenitrile;(5-methyl-1H-imidazol-4-yl)acetonitrile
• CAS NO: 51667-66-4
• Molecular Formula: C₆H₇N₃
• Molecular Weight: 121
• Mol File: 51667-66-4.mol
• Article Data: 6

Chemical Properties

• Melting Point: 163-164 °C
• Boiling Point: 395.2±27.0 °C(Predicted)
• Appearance: /
• Density: 1.170±0.06 g/cm3(Predicted)
• PKA: 13.03±0.10(Predicted)
• CAS DataBase Reference: 2-(5-Methyl-1H-imidazol-4-yl)acetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-Methyl-1H-imidazol-4-yl)acetonitrile(51667-66-4)
• EPA Substance Registry System: 2-(5-Methyl-1H-imidazol-4-yl)acetonitrile(51667-66-4)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 51667-66-4(Hazardous Substances Data)

Usage

General Description

2-(5-Methyl-1H-imidazol-4-yl)acetonitrile is a chemical compound with the molecular formula C7H8N4. It is a nitrile derivative of imidazole, a five-membered heteroaromatic ring containing one nitrogen atom. 2-(5-Methyl-1H-imidazol-4-yl)acetonitrile is commonly used in organic synthesis as a building block for the construction of more complex molecules. It is also known for its potential as a pharmaceutical intermediate, with applications in the development of new drugs. Its structure and reactivity make it suitable for various chemical reactions, making it a valuable reagent in the field of organic chemistry. Additionally, its unique properties and versatile nature make it a valuable tool for researchers and industrial chemists in the development of new materials and pharmaceuticals.

Upstream product

• 151-50-8 potassium cyanide 
• 51605-33-5 4-chloromethyl-5-methyl-imidazole hydrochloride 
• 143-33-9 sodium cyanide 
• 69395-89-7 5-methyl-4-chloromethyl imidazole 
• 29636-87-1 4⁽⁵⁾-methyl-5⁽⁴⁾-hydroxymethylimidazole 
• 51605-33-5 4-methyl-5-chloromethyl-imidazole hydrochloride 
• 60899-79-8 O,S-diethyl-dithiophosphoric acid 

Downstream Products

• 36507-31-0 4-methylhistamine 
• 129486-32-4 4-(2-methoxyphenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-47-1 4-(5-bromo-2-methoxyphenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 124583-51-3 4-phenyl-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 130096-10-5 4-(2-methylphenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-41-5 4-(3-fluorophenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-39-1 4-(3-chlorophenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-30-2 4-(3-bromophenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-33-5 4-(4-fluorophenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-44-8 4-(4-chlorophenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-29-9 4-(2-hydroxyphenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-34-6 4-(2-fluorophenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-28-8 4-(4-methoxyphenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 
• 129486-40-4 4-(3-methoxyphenyl)-2-<<4(5)-methyl-5(4)-imidazolyl>methyl>thiazole 

Relevant articles and documents

5-Substituted imidazole-4-acetic acid analogues: Synthesis, modeling, and pharmacological characterization of a series of novel γ-aminobutyric acidC receptor agonists

A series of ring-substituted analogues of imidazole-4-acetic acid (IAA, 4), a partial agonist at both GABAA and GABAC receptors (GABA = γ-aminobutyric acid), have been synthesized. The synthesized compounds 8a-1 have been evaluated a

ARYLTHIAZOLYLIMIDAZOLES

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Synthesis, in vitro binding profile, and central nervous system penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazol e

4-(2-Methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole (5) is a highly potent member of a structurally novel series of selective serotonin-3 receptor antagonists. The synthesis of tritriated 5 and its binding profile in neuroblastoma-glioma 108