1241777-72-9

Basic information

• Product Name: C₃₅H₃₀BrN₃O₂
• Synonyms: C₃₅H₃₀BrN₃O₂
• CAS NO: 1241777-72-9
• Molecular Weight: 604.546
• Mol File: 1241777-72-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₃₅H₃₀BrN₃O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₅H₃₀BrN₃O₂(1241777-72-9)
• EPA Substance Registry System: C₃₅H₃₀BrN₃O₂(1241777-72-9)

Safety Data

• Hazardous Substances Data: 1241777-72-9(Hazardous Substances Data)

Upstream product

• 77128-73-5 (2S)-N-fluorenylmethyloxycarbonyl-2-amino-N-methyl-3-phenylpropanoic acid 
• 28920-43-6 (fluorenylmethoxy)carbonyl chloride 
• 877-03-2 5-bromo-1H-indole-3-carboxaldehyde 
• 131653-79-7 2-(5'-bromo-3'-indolyl)-1-nitroethene 
• 1241777-71-8 C₃₅H₃₂BrN₃O₃ 

Downstream Products

• 1241777-73-0 C₃₆H₃₄BrN₃O₂ 
• 125443-66-5 eudistomidin B 
• 1384331-20-7 C₃₅H₃₂BrN₃O₂ 
• 1318767-45-1 eudistomidin I 

Relevant articles and documents

Enantioselective total synthesis of eudistomidins G, H, and I

Asymmetric first total synthesis of eudistomidins G, H, and I, tetrahydro-β-carboline alkaloids from the Okinawan marine tunicate Eudistoma glaucus, has been accomplished with the Bischler-Napieralski reaction and the Noyori catalytic asymmetric hydrogen-transfer reaction. The absolute configurations of eudistomidins G, H, and I were confirmed from comparison of the 1H and 13C NMR, and CD spectral data of synthetic and natural eudistomidins G, H, and I, respectively.