877149-13-8

Basic information

• Product Name: 4-Bromo-2-chloro-6-methyl-benzamide
• Synonyms: 4-Bromo-2-chloro-6-methyl-benzamide;BenzaMide, 4-broMo-2-chloro-6-Methyl-
• CAS NO: 877149-13-8
• Molecular Formula: C8H7BrClNO
• Molecular Weight: 248.5
• Mol File: 877149-13-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Bromo-2-chloro-6-methyl-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-2-chloro-6-methyl-benzamide(877149-13-8)
• EPA Substance Registry System: 4-Bromo-2-chloro-6-methyl-benzamide(877149-13-8)

Safety Data

• Hazardous Substances Data: 877149-13-8(Hazardous Substances Data)

Usage

Description

4-Bromo-2-chloro-6-methyl-benzamide is a chemical compound with the molecular formula C8H8BrClNO. It is a benzamide derivative with bromo, chloro, and methyl substituents on the benzene ring. 4-Bromo-2-chloro-6-methyl-benzamide is characterized by its unique structure and reactivity, making it a valuable asset in various applications.

Uses

Used in Organic Synthesis:
4-Bromo-2-chloro-6-methyl-benzamide is used as a building block in organic synthesis for the creation of complex organic molecules. Its unique structure and reactivity allow it to be a key component in the synthesis of various compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Bromo-2-chloro-6-methyl-benzamide is used as an intermediate in the production of various drugs and pharmaceuticals. Its potential applications in the development of new medications for a range of illnesses and conditions make it a promising candidate for further research and development.
Used in Medicinal Chemistry and Drug Discovery:
4-Bromo-2-chloro-6-methyl-benzamide serves as a valuable tool for researchers in medicinal chemistry and drug discovery. Its unique properties and reactivity contribute to the advancement of knowledge in these fields and aid in the identification and development of novel therapeutic agents.
Used as a Reagent in Chemical Reactions:
Due to its unique structure and reactivity, 4-Bromo-2-chloro-6-methyl-benzamide may also have use as a reagent in chemical reactions and organic transformations. This allows for the exploration of new chemical pathways and the development of innovative synthetic methods.