332903-47-6

Basic information

• Product Name: 2-chloro-4-fluoro-6-MethylbenzenaMine
• Synonyms: 2-chloro-4-fluoro-6-MethylbenzenaMine;2-Chloro-4-fluoro-6-methyl-phenylamine;2-Chloro-4-fluoro-6-methylaniline
• CAS NO: 332903-47-6
• Molecular Formula: C₇H₇ClFN
• Molecular Weight: 159.5885832
• Mol File: 332903-47-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-chloro-4-fluoro-6-MethylbenzenaMine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-4-fluoro-6-MethylbenzenaMine(332903-47-6)
• EPA Substance Registry System: 2-chloro-4-fluoro-6-MethylbenzenaMine(332903-47-6)

Safety Data

• Hazardous Substances Data: 332903-47-6(Hazardous Substances Data)

Usage

General Description

"2-chloro-4-fluoro-6-MethylbenzenaMine" is a chemical compound with the molecular formula C7H7ClFN. 2-chloro-4-fluoro-6-MethylbenzenaMine is an organic compound that contains a benzene ring with a chlorine, fluorine, and methyl group attached. It is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. The presence of the chloro and fluoro group in this compound make it useful in various reactions and transformations in organic chemistry. Due to its chemical structure, "2-chloro-4-fluoro-6-MethylbenzenaMine" should be handled and used with caution, following proper safety protocols.

Upstream product

• 326-65-8 N-(4-fluoro-2-methylphenyl)acetamide 
• 452-71-1 4-fluor-2-methylaniline 

Downstream Products

• 332903-61-4 N-(2'-chloro-4'-fluoro-6'-methylphenyl)-4-methylaniline 
• 332903-69-2 2-chloro-N-(2-chloro-4-fluoro-6-methylphenyl)-N-p-tolyl-acetamide 

Relevant articles and documents

SUBSTITUTED AMINOPURINE COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

Provided herein are Aminopurine Compounds having the following structures: wherein R1, R2, and R3 are as defined herein, compositions comprising an effective amount of an Aminopurine Compound, and methods for treating or preventing a cancer, for example, melanoma.

Synthesis of new N-aryl oxindoles as intermediates for pharmacologically active compounds

Various new N-aryl oxindoles were synthesized as intermediates for the preparation of pharmacologically active 2-(N-arylamino)-phenylacetic acids. Two novel approaches were explored for the construction of diarylamine and N-aryl oxindole core structures, in addition to Buchwald-arylamination and Smiles rearrangement. Condensation of anilines with 2-oxo-cyclohexylidene-acetic acid derivatives and subsequent dehydrogenation is a new and viable method for the preparation of N-aryl oxindoles. Graphical Abstract.