72993-43-2

Basic information

• Product Name: (2-Ethyl-1H-iMidazol-5-yl)Methanol
• Synonyms: (2-Ethyl-1H-iMidazol-5-yl)Methanol
• CAS NO: 72993-43-2
• Molecular Formula: C₆H₁₀N₂O
• Molecular Weight: 126.1564
• Mol File: 72993-43-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (2-Ethyl-1H-iMidazol-5-yl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Ethyl-1H-iMidazol-5-yl)Methanol(72993-43-2)
• EPA Substance Registry System: (2-Ethyl-1H-iMidazol-5-yl)Methanol(72993-43-2)

Safety Data

• Hazardous Substances Data: 72993-43-2(Hazardous Substances Data)

Usage

Description

(2-Ethyl-1H-iMidazol-5-yl)Methanol is a chemical compound with the molecular formula C8H12N2O. It is a derivative of imidazole and contains a hydroxymethyl group. (2-Ethyl-1H-iMidazol-5-yl)Methanol is commonly used as a building block in organic synthesis and pharmaceutical manufacturing.

Uses

Used in Pharmaceutical Manufacturing:
(2-Ethyl-1H-iMidazol-5-yl)Methanol is used as a building block for the development of new drugs and treatments. Its unique structure and properties make it a valuable component in the creation of various pharmaceutical compounds.
Used in Agriculture:
(2-Ethyl-1H-iMidazol-5-yl)Methanol is used as an antimicrobial agent in agriculture. Its antifungal and antibacterial properties make it useful in the development of treatments for plant diseases and pests.
Used in Veterinary Medicine:
(2-Ethyl-1H-iMidazol-5-yl)Methanol is used as an antimicrobial agent in veterinary medicine. Its potential to combat infections in animals makes it a valuable tool in the development of treatments for various animal diseases.
Used in Organic Synthesis:
(2-Ethyl-1H-iMidazol-5-yl)Methanol is used as a building block in organic synthesis. Its unique structure and properties make it a versatile component in the creation of various organic compounds for research and industrial applications.

Upstream product

• 96-26-4 dihydroxyacetone 
• 123-38-6 propionaldehyde 

Downstream Products

• 146650-76-2 Ethyl 1-[[3-bromo-2-[2-[[(trifluoromethyl)sulphonyl]amino]phenyl]-5-benzofuranyl]methyl]-4-chloro-2-ethyl-1H-imidazole-5-carboxylate 
• 146650-71-7 ethyl 1-[[3-bromo-2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]phenyl]-5-benzofuranyl]methyl]-4-chloro-2-ethyl-1H-imidazole-5-carboxylate 
• 146650-79-5 1-[[3-Bromo-2-[2-[[(trifluoromethyl)sulphonyl]amino]phenyl]-5-benzofuranyl]methyl]-4-chloro-2-ethyl-1H-imidazole-5-carboxylic acid 
• 145824-18-6 3-[3-Bromo-2-(2-tert-butoxycarbonylamino-phenyl)-benzofuran-5-ylmethyl]-5-chloro-2-ethyl-3H-imidazole-4-carboxylic acid 
• 145824-16-4 1-[[3-Bromo-2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]phenyl]-5-benzofuranyl]methyl]-4-chloro-2-ethyl-1H-imidazole-5-carboxaldehyde 
• 146650-73-9 ethyl 1-[[3-bromo-2-(2-aminophenyl)-5-benzofuranyl]methyl]-4-chloro-2-ethyl-1H-imidazole-5-carboxylate 
• 146650-65-9 2-ethyl-4-chloro-5-(hydroxymethyl)-imidazole 

Relevant articles and documents

Design, synthesis, and calcium channel antagonist activity of new 1,4-dihydropyridines containing 4-(5)-chloro-2-ethyl-5-(4)-imidazolyl substituent

A series of dialkyl, dicycloalkyl, and diaryl ester analogues of nifedipine, in which the ortho-nitro phenyl group at position 4 is replaced by the 4-(5)-chloro-2-ethyl-5-(4)-imidazolyl substituent, were synthesized and evaluated as calcium channel antago