51333-64-3

Basic information

• Product Name: 2-Acetyl-5-broMopyrrole
• Synonyms: 2-Acetyl-5-broMopyrrole;1-(4-bromo-1H-pyrrol-2-yl)ethanone
• CAS NO: 51333-64-3
• Molecular Formula: C₆H₆BrNO
• Molecular Weight: 188.02194
• Mol File: 51333-64-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Acetyl-5-broMopyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Acetyl-5-broMopyrrole(51333-64-3)
• EPA Substance Registry System: 2-Acetyl-5-broMopyrrole(51333-64-3)

Safety Data

• Hazardous Substances Data: 51333-64-3(Hazardous Substances Data)

Usage

Chemical Structure

Brominated derivative of pyrrole

Usage

Creation of pharmaceuticals, perfumes, specialty chemicals

Odor

Distinctive

Application

Flavor and fragrance agent

Study

Potential applications in organic synthesis and materials science

Properties

Valuable building block in chemical production.

Upstream product

• 123-91-1 1,4-dioxane 
• 1072-83-9 2-Acetylpyrrole 
• 7726-95-6 bromine 

Relevant articles and documents

HETEROARYL COMPOUNDS FOR TREATING HUNTINGTON'S DISEASE

The present description relates to compounds, forms, and pharmaceutical compositions thereof and methods of using such compounds, forms, or compositions thereof for treating or ameliorating Huntington's disease. In particular, the present description relates to substituted benzothiazole compounds of Formula (I) or (II), forms and pharmaceutical compositions thereof and methods of using such compounds, forms, or compositions thereof for treating or ameliorating Huntington's disease.

COMPOUNDS FOR TREATING HUNTINGTON'S DISEASE

The present description relates to compounds, forms, and pharmaceutical compositions thereof and methods of using such compounds, forms, or compositions thereof for treating or ameliorating Huntington's disease. In particular, the present description relates to substituted bicyclic heteroaryl compounds of Formula (I), forms and pharmaceutical compositions thereof and methods of using such compounds, forms, or compositions thereof for treating or ameliorating Huntington's disease.

Selective bromination of pyrrole derivatives, carbazole and aromatic amines with DMSO/HBr under mild conditions

Bromination of pyrrole derivatives, carbazole and aromatic amines using the DMSO/HBr system affords high yields of the corresponding bromo compounds. Temperature control used in the bromination of anilines helped to promote selective formation of mono- or di-brominated products. Simple operation, low toxicity and high selectivity make this a promising new procedure for the bromination of aromatic compounds.