1313710-72-3

Basic information

• Product Name: (S)-3-(9-fluorenylmethoxycarbonylamino)-2-(6-fluoro-1H-indol-3-yl)propionic acid
• CAS NO: 1313710-72-3
• Molecular Weight: 444.462
• Mol File: 1313710-72-3.mol

Chemical Properties

• CAS DataBase Reference: (S)-3-(9-fluorenylmethoxycarbonylamino)-2-(6-fluoro-1H-indol-3-yl)propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-(9-fluorenylmethoxycarbonylamino)-2-(6-fluoro-1H-indol-3-yl)propionic acid(1313710-72-3)
• EPA Substance Registry System: (S)-3-(9-fluorenylmethoxycarbonylamino)-2-(6-fluoro-1H-indol-3-yl)propionic acid(1313710-72-3)

Safety Data

• Hazardous Substances Data: 1313710-72-3(Hazardous Substances Data)

Upstream product

• 399-51-9 6-fluoro-1H-indole 
• 1313710-55-2 [N-(4-benzyloxycarbonylphenyl)-4,4-dimethyl-2-oxopyrrolidin-3-yl] (3'R,2S)-2-(6-fluoro-1H-indol-3-yl)-3-nitropropionate 
• 1313710-64-3 [N-(4-carboxyphenyl)-4,4-dimethyl-2-oxopyrrolidin-3-yl] (3'R,2S)-2-(6-fluoro-1H-indol-3-yl)-3-aminopropionate acetate 
• 1313710-71-2 C₃₉H₃₄FN₃O₇ 

Relevant articles and documents

Asymmetric synthesis of β2-tryptophan analogues via Friedel-Crafts alkylation of indoles with a chiral nitroacrylate

The asymmetric Friedel-Crafts alkylation of various indoles with a chiral nitroacrylate provides optically active β-tryptophan analogues after reduction of the nitro group and removal of the chiral auxiliary. This reaction generally occurs in good yield a