1384331-21-8

Basic information

• Product Name: C₃₇H₃₆BrN₃O₃
• CAS NO: 1384331-21-8
• Molecular Weight: 650.615
• Mol File: 1384331-21-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₇H₃₆BrN₃O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₇H₃₆BrN₃O₃(1384331-21-8)
• EPA Substance Registry System: C₃₇H₃₆BrN₃O₃(1384331-21-8)

Safety Data

• Hazardous Substances Data: 1384331-21-8(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 1384331-18-3 C₃₅H₃₂BrN₃O₂ 
• 319493-07-7 3-(2-nitrovinyl)-6-bromo-1H-indole 
• 1384331-17-2 C₃₅H₃₂BrN₃O₃ 
• 1384331-16-1 C₃₅H₃₀BrN₃O₂ 
• 17826-04-9 6-bromo-1H-indole-3-carbaldehyde 
• 28920-43-6 (fluorenylmethoxy)carbonyl chloride 
• 35661-40-6 N-Fmoc L-Phe 
• 84000-03-3 9H-fluoren-9-ylmethyl (S)-4-benzyl-5-oxo-1,3-oxazolidine-3-carboxylate 
• 77128-73-5 (2S)-N-fluorenylmethyloxycarbonyl-2-amino-N-methyl-3-phenylpropanoic acid 
• 96624-18-9 6-bromotryptamine 

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.