70122-99-5

Basic information

• Product Name: [2,2,2-Trichloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid methyl ester
• Synonyms: [2,2,2-Trichloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid methyl ester
• CAS NO: 70122-99-5
• Molecular Weight: 316.999
• Mol File: 70122-99-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [2,2,2-Trichloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [2,2,2-Trichloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid methyl ester(70122-99-5)
• EPA Substance Registry System: [2,2,2-Trichloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid methyl ester(70122-99-5)

Safety Data

• Hazardous Substances Data: 70122-99-5(Hazardous Substances Data)

Upstream product

• 25801-41-6 (2,2,2-Trichloro-1-methoxycarbonylamino-ethyl)-carbamic acid methyl ester 
• 108-90-7 chlorobenzene 

Downstream Products

• 77429-29-9 2,2-Dichloro-1-(4-chloro-phenyl)-ethylamine; hydrochloride 
• 77429-33-5 phenyl N-(2,2-dichloro-1-chlorophenylethyl)carbamate 
• 77429-20-0 [2,2-Dichloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid ethyl ester 
• 77429-25-5 1-Chloro-4-(2,2-dichloro-1-isocyanato-ethyl)-benzene 
• 75119-75-4 4-(4-Chloro-phenyl)-4-trichloromethyl-3,4-dihydro-pyrido[1,2-a][1,3,5]triazin-2-one 
• 75119-63-0 [2,2,2-Trichloro-1-(4-chloro-phenyl)-eth-(E)-ylidene]-carbamic acid phenyl ester 
• 75119-84-5 1-Chloro-4-(1,2,2,2-tetrachloro-1-isocyanato-ethyl)-benzene 
• 77429-19-7 [2,2-Dichloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid methyl ester 
• 75119-81-2 [1,2,2,2-Tetrachloro-1-(4-chloro-phenyl)-ethyl]-carbamic acid methyl ester 
• 7138-34-3 p-chloromandelic acid 

Relevant articles and documents

SYNTHESIS AND SOME PROPERTIES OF 1,1-DI(ALKOXYCARBONYLAMINO)-2,2-DIHALOGENO- AND 1,1-DI(ALKOXYCARBONYLAMINO)-2,2,2-TRIHALOGENOETHANES

1,1-Di(alkoxycarbonylamino)-2,2,2-trihalogenoethanes were obtained by heating trihalogenoacetaldehydes or their hydrates with urethanes in a ratio of 1:2 in the presence of catalytic amounts of concentrated sulfuric acid.The products were reduced selectively with aluminum amalgam in 90percent alcohol to 1,1-di(alkoxycarbonylamino)-2,2-dihalogenoethanes.Compounds of both types react smoothly with benzene and its homologs in the presence of concentrated sulfuric acid and give 1-alkoxycarbonylamino-1-aryl-2,2-dihalogeno- and 1-alkoxycarbonylamino-1-aryl-2,2,2-trihalogenoethanes respectively.In an alkaline medium the latter are cleaved to aryloxyacetic acid, and with phosphorus pentachloride they form 1-aryl-2,2-dihalogeno- and 1-aryl-2,2,2-trihalogenoethyl isocyanates.