| Identification | Back Directory | [Name]
ETHYL 4-(2-CHLOROACETAMIDO)BENZOATE | [CAS]
26226-72-2 | [Synonyms]
AKOS B015654
AKOS USSH-4110488
AKOS BBS-00003983
BUTTPARK 80\07-83
TIMTEC-BB SBB003207
LABOTEST-BB LT00452438
ETHYL 4-(2-CHLOROACETAMIDO)BENZOATE
Ethyl p-(chloroacetylamino) benzoate
ETHYL 4-[(CHLOROACETYL)AMINO]BENZOATE
ethyl 4-(2-chloroethanoylamino)benzoate
ETHYL 4-[(2-CHLOROACETYL)AMINO]BENZOATE
p-Chloroacetylaminobenzoic acid ethyl ester
Benzoic acid, p-(2-chloroacetamido)-, ethyl ester
Benzoic acid, 4-[(chloroacetyl)aMino]-, ethyl ester
JR-8639, Ethyl 4-[(chloroacetyl)amino]benzoate, 97%
BENZOIC ACID, 4-[(2-CHLOROACETYL)AMINO]-, ETHYL ESTER
4-[(2-chloro-1-oxoethyl)amino]benzoic acid ethyl ester | [Molecular Formula]
C11H12ClNO3 | [MDL Number]
MFCD00018909 | [MOL File]
26226-72-2.mol | [Molecular Weight]
241.67 |
| Hazard Information | Back Directory | [General Description]
Ethyl 4-(2-chloroacetamido)benzoate can be synthesized starting from benzocaine. It undergoes heterocyclization in the presence of ammonium thiocyanate in refluxing ethanol to afford ethyl-4-(4-oxothiazolidin-2-ylideneamino)benzoate, via intramolecular cyclization and the Dimroth-like rearrangements. |
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