129604-31-5

Basic information

• Product Name: Ethanone, 2-chloro-1-(2,4,5-trifluorophenyl)- (9CI)
• Synonyms: Ethanone, 2-chloro-1-(2,4,5-trifluorophenyl)- (9CI)
• CAS NO: 129604-31-5
• Molecular Formula: C₈H₄ClF₃O
• Molecular Weight: 208.5649696
• Product Categories: ACETYLHALIDE
• Mol File: 129604-31-5.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanone, 2-chloro-1-(2,4,5-trifluorophenyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-chloro-1-(2,4,5-trifluorophenyl)- (9CI)(129604-31-5)
• EPA Substance Registry System: Ethanone, 2-chloro-1-(2,4,5-trifluorophenyl)- (9CI)(129604-31-5)

Safety Data

• Hazardous Substances Data: 129604-31-5(Hazardous Substances Data)

Upstream product

• 367-23-7 1,2,4-trifluorobenzene 
• 79-04-9 chloroacetyl chloride 
• 129322-83-4 2',4',5'-trifluoroacetophenone 

Downstream Products

• 209995-38-0 (2,4,5-trifluorophenyl)acetic acid 
• 1000180-66-4 1-chloro-2-(2,4,5-trifluorophenyl)-3-(4-fluorophenyl)propan-2-ol 
• 446-17-3 2,4,5-trifluorobenzoic acid 

Relevant articles and documents

NEW PROCESS FOR THE PREPARATION OF 2,4,5- TRIFLUOROPHENYLACETIC ACID"

The present invention relates to a new process for the preparation of 2,4,5-trifluorophenylacetic acid and salts thereof by means of new synthetic intermediates.

Antimycotically active substituted 2-aminothiazoles

Antimicotically active 2-aminothiazoles have been found having the formula STR1 in which R1 represents hydrogen or alkyl and R2 represents optionally substituted cyclohexyl or phenyl which is substituted by halogen, alkyl, halogenoalkyl, halogenoalkoxy, dioxyhalogenoalkyl or halogenoalkylthio, and their physiologically tolerable acid addition salts, with the exception of the compounds 4-(4-chlorophenyl)-2-[2-(1,4,5,6-tetrahydropyrimidinyl)-amino]thiazole and 4-(2,4-dichlorophenyl)-2-[2-(1,4,5,6-tetrahydropyrimidinyl)-amino]-thiazole and 4-(4-chloro-2-methylphenyl)-2-[2-(1,4,5,6-tetrahydropyrimidinyl)-amino]-thiazole and with the exception of the physiologically tolerable acid addition salts of these compounds have been found.

Process for the preparation of fluorinated benzoic acids

In the process for the preparation of fluorinated benzoic acids of the formula I STR1 in which X and Y, for example, independently of one another denote chlorine or fluorine and X moreover denotes bromine, a fluorinated chloroacetophenone of the formula II STR2 in which Z denotes chlorine or hydrogen, is reacted with a hypohalite.