102939-46-8

Basic information

• Product Name: Hexanoic acid, 6-chloro-6-oxo-
• CAS NO: 102939-46-8
• Molecular Formula: C6H9ClO3
• Molecular Weight: 164.589
• Mol File: 102939-46-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Hexanoic acid, 6-chloro-6-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Hexanoic acid, 6-chloro-6-oxo-(102939-46-8)
• EPA Substance Registry System: Hexanoic acid, 6-chloro-6-oxo-(102939-46-8)

Safety Data

• Hazardous Substances Data: 102939-46-8(Hazardous Substances Data)

Upstream product

• 124-04-9 Adipic acid 

Downstream Products

• 7029-26-7 1,6-diphenyl-hexane-1,6-dione dioxime 
• 146929-48-8 -6-<<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-6-oxohexanoic acid monohydrochloride 
• 146953-17-5 -6-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-6-oxohexanoic acid 
• 146953-21-1 <2R-(2R*,6R*)>-2-(1H-indol-3-ylmethyl)-2-methyl-6-phenyl-1,4,7-triazacyclotridecan-3,8,13-trione 
• 3375-38-0 1,4-dibenzoylbutane 
• 148556-76-7 methyl -6-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-6-oxohexanoate 

Relevant articles and documents

PROCESS FOR PRODUCING CARBOXYLIC ACID CHLORIDE

This invention relates to a method for producing a carboxylic acid chloride, which efficiently decomposes a Vilsmeier reagent type compound in a carboxylic acid chloride lacking a thermal stability or a carboxylic acid chloride hardly distilled in practice due to a high boiling point with a simple operation and has no adverse effect on a subsequent step, and more particularly to a method for producing a carboxylic acid chloride, characterized by comprising reacting a carboxylic acid with a chlorinating agent in the presence of a catalyst, removing the excessive chlorinating agent from a reaction system after the reaction, and then further adding 1.0 to 3.0 equivalents of the starting carboxylic acid based on the catalyst to the reaction system to decompose a Vilsmeier reagent type compound remaining in the reaction system.