195134-70-4

Basic information

• Product Name: Carbamic acid, (3,5-dibromophenyl)-, 1,1-dimethylethyl ester
• CAS NO: 195134-70-4
• Molecular Formula: C11H13Br2NO2
• Molecular Weight: 351.038
• Mol File: 195134-70-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (3,5-dibromophenyl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (3,5-dibromophenyl)-, 1,1-dimethylethyl ester(195134-70-4)
• EPA Substance Registry System: Carbamic acid, (3,5-dibromophenyl)-, 1,1-dimethylethyl ester(195134-70-4)

Safety Data

• Hazardous Substances Data: 195134-70-4(Hazardous Substances Data)

Upstream product

• 618-58-6 3,5-dibromobenzoic acid 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 195134-82-8 2-Diazo-N-(3,5-dibromo-phenyl)-N-(4-methoxy-benzyl)-malonamic acid ethyl ester 
• 195134-83-9 4,6-Dibromo-1-(4-methoxy-benzyl)-2-oxo-2,3-dihydro-1H-indole-3-carboxylic acid ethyl ester 
• 195134-84-0 4,6-Dibromo-1-(4-methoxy-benzyl)-3-methyl-2-oxo-2,3-dihydro-1H-indole-3-carboxylic acid ethyl ester 
• 195134-75-9 N-Benzyl-2-diazo-N-(3,5-dibromo-phenyl)-malonamic acid ethyl ester 
• 195134-93-1 4,6-dibromo-1-(4-methoxybenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl acetate 
• 195134-76-0 1-Benzyl-4,6-dibromo-2-oxo-2,3-dihydro-1H-indole-3-carboxylic acid ethyl ester 
• 195134-77-1 1-Benzyl-4,6-dibromo-3-methyl-2-oxo-2,3-dihydro-1H-indole-3-carboxylic acid ethyl ester 
• 195134-85-1 4,6-dibromo-3-hydroxy-1-(4-methoxybenzyl)-3-methylindolin-2-one 
• 195134-81-7 3,5-dibromo-N-(4-methoxybenzyl)aniline 
• 195134-74-8 N-benzyl-3,5-dibromoaniline 
• 195134-80-6 3,5-dibromo-N-(tert-butoxycarbonyl)-N-(4-methoxybenzyl)aniline 
• 195134-73-7 N-benzyl-3,5-dibromo-N-(tert-butoxycarbonyl)aniline 

Relevant articles and documents

Synthesis of the marine dibromooxoindoline convolutamydine C

A synthesis of the marine 4,6-dibromo-3-hydroxyoxoindoline convolutamydine C 3 is described. The key steps are the rhodium(II) perfluorobutyramide catalysed cyclisation of diazoamide 17 to give the oxoindoline 18, and the subsequent high yielding one-pot hydrolysis-decarboxylation-oxidation of 19 to 20. X-Ray crystal structures have been determined for the diazoamides 10 and 17 and for the oxoindolines 11 and 13.