5255-70-9

Basic information

• Product Name: Carbamic acid, (2-chlorophenyl)-, ethyl ester
• CAS NO: 5255-70-9
• Molecular Formula: C9H10ClNO2
• Molecular Weight: 199.637
• Mol File: 5255-70-9.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (2-chlorophenyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (2-chlorophenyl)-, ethyl ester(5255-70-9)
• EPA Substance Registry System: Carbamic acid, (2-chlorophenyl)-, ethyl ester(5255-70-9)

Safety Data

• Hazardous Substances Data: 5255-70-9(Hazardous Substances Data)

Upstream product

• 13208-19-0 N,N'-bis(2-chlorophenyl)urea 
• 95-92-1 oxalic acid diethyl ester 
• 64-17-5 ethanol 
• 1202047-19-5 1-tert-butyl-1-isopropyl-3-phenylurea 
• 101-99-5 N-carboethoxyaniline 
• 108-90-7 chlorobenzene 
• 51-79-6 urethane 
• 124-38-9 carbon dioxide 
• 75-03-6 ethyl iodide 
• 95-51-2 o-chloroaniline 
• 201230-82-2 carbon monoxide 
• 88-73-3 2-Chloronitrobenzene 
• 541-41-3 chloroformic acid ethyl ester 
• 3320-83-0 o-chlorophenyl isocyanate 

Downstream Products

• 1349807-28-8 (S)-ethyl 2-chloro-4-(2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenylcarbamate 
• 1349807-89-1 ethyl 2-chloro-4-sulfamoylphenylcarbamate 
• 1349807-71-1 ethyl 2-chloro-4-(chlorosulfonyl)phenylcarbamate 
• 23441-75-0 4-phenyl-1H-quinazolin-2-one 
• 444901-13-7 ethyl 2-chlorophenyl[2,4-dinitro-6-(trifluoromethyl)phenyl]carbamate 

Relevant articles and documents

Nickel(II)- And Silver(I)-Catalyzed C-H Bond Halogenation of Anilides and Carbamates

ortho -C-H bond halogenation of anilides and N -aryl carbamates using easily available N -halosuccinimides (NXS) as the active halogenation reagent in the presence of nickel or silver catalyst has been developed. This method provides a new approach to 2-haloanilides and carbamates, which may serve as starting materials for the synthesis of pharmaceutically and biologically active compounds.

Structure-activity relationship study of arylsulfonylimidazolidinones as anticancer agents

In an effort to find novel N-arylsulfonylimidazolidinones as highly potent anticancer agent, the structure-activity relationship of ethyl 2-methyl-4-(2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenylcarbamate was explored through synthesis and evaluation of

Facile double-lithiation of a transient urea: Vicarious ortho -metalation of aniline derivatives

A convenient one-pot method for the conversion of phenylisocyanate into ortho-functionalized aniline derivatives has been developed. The reaction proceeds via the selective ortho-metalation of a transient labile urea, which can be considered as a synthetic equivalent of 2-lithio-phenylisocyanate, a highly improbable intermediate.