Atomfair p-Chlorophenacyl bromide C8H6BrClO

Description p-Chlorophenacyl bromide (CAS No. 536-38-9) is a high-purity organic compound with the molecular formula C8H6BrClO, widely utilized in synthetic chemistry and pharmaceutical research. This crystalline solid, also known as 2-bromo-1-(4-chlorophenyl)ethanone, serves as a versatile alkylating agent and intermediate in the preparation of heterocyclic compounds, fine chemicals, and bioactive molecules. Its reactive ??-bromo ketone moiety enables efficient nucleophilic substitution reactions, making it invaluable for constructing complex molecular architectures. Suitable for laboratory and industrial-scale applications, our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in securely sealed amber vials to maintain stability. Store at 2-8??C in a…

Description

p-Chlorophenacyl bromide (CAS No. 536-38-9) is a high-purity organic compound with the molecular formula C₈H₆BrClO, widely utilized in synthetic chemistry and pharmaceutical research. This crystalline solid, also known as 2-bromo-1-(4-chlorophenyl)ethanone, serves as a versatile alkylating agent and intermediate in the preparation of heterocyclic compounds, fine chemicals, and bioactive molecules. Its reactive ??-bromo ketone moiety enables efficient nucleophilic substitution reactions, making it invaluable for constructing complex molecular architectures. Suitable for laboratory and industrial-scale applications, our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in securely sealed amber vials to maintain stability. Store at 2-8??C in a dry environment to prevent degradation.

CAS No: 536-38-9
Molecular Formula: C8H6BrClO
Molecular Weight: 233.49
Exact Mass: 231.92906
Monoisotopic Mass: 231.92906
IUPAC Name: 2-bromo-1-(4-chlorophenyl)ethanone
SMILES: C1=CC(=CC=C1C(=O)CBr)Cl
Synonyms: 536-38-9, 2-Bromo-4′-chloroacetophenone, 2-Bromo-1-(4-chlorophenyl)ethanone, p-Chlorophenacyl bromide, Ethanone, 2-bromo-1-(4-chlorophenyl)-

Application

p-Chlorophenacyl bromide is extensively employed as a key intermediate in organic synthesis, particularly for the preparation of pharmaceuticals and agrochemicals. Researchers utilize it in the derivatization of carboxylic acids via phenacyl ester formation for analytical applications. Its reactivity as an alkylating agent also facilitates the synthesis of heterocycles such as pyrazoles and imidazoles. Additionally, this compound finds use in photoaffinity labeling studies due to its UV-sensitive bromoketone group.

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