CAS 61985-25-9

4-Acetylimidazole

Description:

4-Acetylimidazole is an organic compound characterized by its imidazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. This compound features an acetyl group attached to the fourth position of the imidazole ring, contributing to its reactivity and potential applications. It is typically a white to off-white solid, soluble in polar solvents such as water and alcohols, and exhibits moderate stability under standard conditions. 4-Acetylimidazole can participate in various chemical reactions, including acylation and condensation, making it useful in organic synthesis and pharmaceutical applications. Its unique structure allows it to act as a building block for more complex molecules, and it may also exhibit biological activity, which is of interest in medicinal chemistry. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken. Overall, 4-acetylimidazole is a versatile compound with significant potential in both research and industrial applications.

Formula: C₅H₇ClN₂O

InChI: InChI=1/C5H6N2O.ClH/c1-4(8)5-2-6-3-7-5;/h2-3H,1H3,(H,6,7);1H

SMILES: CC(=O)c1cnc[nH]1.Cl

Synonyms:

• 1-(1H-Imidazol-4-Yl)-Ethanone Hcl

1-(1H-IMIDAZOL-4-YL)-ETHANONE HCL

CAS: 61985-25-9

Formula: C₅H₆N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 110.1139

Ref: IN-DA00EARM

4-Acetylimidazole

CAS: 61985-25-9

4-Acetylimidazole

Purity: 95%

Molecular weight: 110.11g/mol

Ref: 54-OR1011397

4-Acetylimidazole

CAS: 61985-25-9

Formula: C₅H₆N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 110.116

Ref: 10-F036623

1-(1H-imidazol-4-yl)ethanone

Controlled Product

CAS: 61985-25-9

Formula: C₅H₆N₂O

Color and Shape: Neat

Molecular weight: 110.11

Ref: TR-I385615

4-Acetylimidazole

CAS: 61985-25-9

4-Acetylimidazole is a histidine analogue that has been shown to have anticancer activity in breast cancer cells. It can react with amines and form imidazoles. The hydroxyl group on the 4-position of the imidazole ring is able to undergo dehydration, which leads to the formation of a chloride ion. This reaction mechanism is reversible and can be used in organic synthesis. 4-Acetylimidazole can also act as an h2 receptor antagonist, although it does not bind to the zwitterionic site of the h2 receptor. NMR spectra show that 4-acetylimidazole exists as a zwitterion in water solution, but becomes a monovalent ion when dissolved in an organic solvent such as methanol or acetone. 4-Acetylimidazole is chemically stable and does not react with poloxamer.

Formula: C₅H₆N₂O

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 110.11 g/mol

Ref: 3D-FA45211