1573112-29-4

Basic information

• Product Name: methyl 3-(4-bromophenyl)-3a,4-dimethyl-3,3a,4,8b-tetrahydrocyclopenta[b]indole-1-carboxylate
• Synonyms: methyl 3-(4-bromophenyl)-3a,4-dimethyl-3,3a,4,8b-tetrahydrocyclopenta[b]indole-1-carboxylate
• CAS NO: 1573112-29-4
• Molecular Weight: 398.299
• Mol File: 1573112-29-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 3-(4-bromophenyl)-3a,4-dimethyl-3,3a,4,8b-tetrahydrocyclopenta[b]indole-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(4-bromophenyl)-3a,4-dimethyl-3,3a,4,8b-tetrahydrocyclopenta[b]indole-1-carboxylate(1573112-29-4)
• EPA Substance Registry System: methyl 3-(4-bromophenyl)-3a,4-dimethyl-3,3a,4,8b-tetrahydrocyclopenta[b]indole-1-carboxylate(1573112-29-4)

Safety Data

• Hazardous Substances Data: 1573112-29-4(Hazardous Substances Data)

Upstream product

• 68267-69-6 N-acetyl-2-allylaniline 
• 875-79-6 1,2-dimethylindole 
• 272456-69-6 (E)-methyl 2-diazo-4-(4-bromophenyl)but-3-enoate 
• 95-20-5 2-methyl-1H-indole 
• 37842-85-6 1-acetyl-2-methylindole 
• 103-84-4 Acetanilid 
• 169214-12-4 [2'-²H]acetanilide 

Relevant articles and documents

Synthesis of indoles through Rh(III)-catalyzed C-H cross-coupling with allyl carbonates

A practical Rh-catalyzed reaction was developed to achieve 2-alkyl-substituted indole synthesis. The reaction can tolerate a variety of synthetically important functional groups. The indole products can also be transformed into other important skeletons. Two bioactive compounds, that is indomethacin and pravadoline were prepared using the new method.