209168-88-7

Basic information

• Product Name: Carbamic acid, [2-(6-bromo-1H-indol-3-yl)ethyl]-, 1,1-dimethylethyl ester
• Synonyms: Carbamic acid, N-[2-(6-bromo-1H-indol-3-yl)ethyl]-, 1,1-dimethylethyl ester;Carbamic acid, [2-(6-bromo-1H-indol-3-yl)ethyl]-, 1,1-dimethylethyl ester (9CI)
• CAS NO: 209168-88-7
• Molecular Formula: C15H19BrN2O2
• Molecular Weight: 339.22800
• Mol File: 209168-88-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-(6-bromo-1H-indol-3-yl)ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-(6-bromo-1H-indol-3-yl)ethyl]-, 1,1-dimethylethyl ester(209168-88-7)
• EPA Substance Registry System: Carbamic acid, [2-(6-bromo-1H-indol-3-yl)ethyl]-, 1,1-dimethylethyl ester(209168-88-7)

Safety Data

• Hazardous Substances Data: 209168-88-7(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 5548-10-7 indole-3-glyoxylamide 

Downstream Products

• 1395418-76-4 (3aR,8aR)-tert-butyl 6-bromo-3a,8-bis(3-oxo-3-phenylpropyl)-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1(2H)-carboxylate 
• 1395418-86-6 C₃₄H₃₀BrN₃O₆S 
• 108061-77-4 6-bromotryptamine hydrochloride 

Relevant articles and documents

Synthesis of the brominated marine alkaloids (±)-arborescidine A, B and C

A straightforward synthesis of the brominated marine alkaloids arborescidine A (1), B (2) and C (3), starting from 6-bromo-(N-methyl) trypatamine is described. An equilibrium, under both basic and acidic conditions was found to exist between the trans- and cis-isomers 3 and 4. Spectral data indicated that the structure of isomer 4 does not correspond with the compound identified as arborescidine D recently isolated from the marine tunicate Pseudodistoma arborescens.