129643-72-7

Basic information

• Product Name: 1-(5-chloro-2-(4-chlorophenoxy)phenyl)ethanone
• Synonyms: 1-(5-chloro-2-(4-chlorophenoxy)phenyl)ethanone
• CAS NO: 129643-72-7
• Molecular Weight: 281.138
• Mol File: 129643-72-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(5-chloro-2-(4-chlorophenoxy)phenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5-chloro-2-(4-chlorophenoxy)phenyl)ethanone(129643-72-7)
• EPA Substance Registry System: 1-(5-chloro-2-(4-chlorophenoxy)phenyl)ethanone(129643-72-7)

Safety Data

• Hazardous Substances Data: 129643-72-7(Hazardous Substances Data)

Upstream product

• 2476-37-1 2,5-dichloroacetophenone 
• 1193-00-6 sodium 4-chlorophenolate 
• 5780-37-0 (E)-acetaldoxime 
• 121-27-7 2-(4'-chlorophenoxy)-5-chloro-aniline 
• 7758-99-8 copper(II) sulfate 
• 7757-82-6 sodium sulfate 

Downstream Products

• 3380-53-8 Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester 
• 57388-57-5 2-(4-chloro-phenoxy)-5-chloro-phenylacetic acid 

Relevant articles and documents

Process for the preparation of halogenated hydroxydiphenyl compounds

A process for the preparation of halohydroxydiphenyl compounds useful for protecting organic materials and articles from microorganisms, of the formula by acylation of a halogenated benzene compound (first stage), etherification of the acylated compound with a halogenated phenol compound (second stage), oxidation of the etherified compound (third stage) and hydrolysis of the oxidized compound in a fourth stage, according to the following reaction scheme: in which R1 and R2 independently of one another are F, Cl or Br; R3 and R4 independently of one another are hydrogen; or C1-C4alkyl; m is 1 to 3; and n is 1 or 2.

Substituted (2-Phenoxyphenyl)acetic Acids with Antiinflammatory Activity. 1

The synthesis and antiinflammatory activity of a series of substituted (2-phenoxyphenyl)acetic acids are described.Initial screening in the adjuvant arthritis test showed that halogen substitution in the phenoxy ring enhanced activity considerably.Ulcerogenic potential, as measured by the minimum ulcerogenic dose (MUD), was low in almost all the acids tested. acetic acid possessed the most favorable combination of potency with low toxicity, including ulcerogenicity, and this compound is now in therapeutic use.