185142-08-9

Basic information

• Product Name: Heptanoic acid, 6,6-dimethyl-5-oxo-2-[(9-phenyl-9H-fluoren-9-yl)amino]-, methyl ester, (2S)-
• CAS NO: 185142-08-9
• Molecular Formula: C29H31NO3
• Molecular Weight: 441.57
• Mol File: 185142-08-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Heptanoic acid, 6,6-dimethyl-5-oxo-2-[(9-phenyl-9H-fluoren-9-yl)amino]-, methyl ester, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Heptanoic acid, 6,6-dimethyl-5-oxo-2-[(9-phenyl-9H-fluoren-9-yl)amino]-, methyl ester, (2S)-(185142-08-9)
• EPA Substance Registry System: Heptanoic acid, 6,6-dimethyl-5-oxo-2-[(9-phenyl-9H-fluoren-9-yl)amino]-, methyl ester, (2S)-(185142-08-9)

Safety Data

• Hazardous Substances Data: 185142-08-9(Hazardous Substances Data)

Upstream product

• 185142-04-5 (2S,4RS)-6,6-dimethyl-5-oxo-4-<(methyloxy)carbonyl>-2-heptanoic acid 
• 119595-72-1 L-N-(9-(9-phenylfluorenyl))glutamic acid γ-methylester 
• 3282-30-2 pivaloyl chloride 
• 185142-06-7 (S)-6,6-Dimethyl-5-oxo-2-(9-phenyl-9H-fluoren-9-ylamino)-heptanoic acid 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 

Downstream Products

• 185142-15-8 (2S,5R)-N-(tert-butyloxycarbonyl)-5-tert-butylproline 
• 185142-33-0 (S)-6,6-Dimethyl-5-oxo-2-(9-phenyl-9H-fluoren-9-ylamino)-heptanoic acid methylamide 
• 366482-56-6 7-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-(9-phenyl-9H-fluoren-9-ylamino)-heptan-3-one 
• 366482-55-5 7-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-6-(9-phenyl-9H-fluoren-9-ylamino)-heptan-3-ol 
• 366482-54-4 6,6-dimethyl-2-(9-phenyl-9H-fluoren-9-ylamino)-heptane-1,5-diol 
• 185142-06-7 (S)-6,6-Dimethyl-5-oxo-2-(9-phenyl-9H-fluoren-9-ylamino)-heptanoic acid 

Relevant articles and documents

Racemization in the use of N-(9-(9-phenylfluorenyl))serine-derived cyclic sulfamidates in the synthesis of delta-keto alpha-amino carboxylates and prolines.

[reaction: see text]Ring opening of enantiopure N-(9-(9-phenylfluorenyl)serine-derived cyclic sulfamidates with beta-keto esters, beta-keto ketones, and dimethyl malonate gave a variety of gamma-substituted amino acid analogues in racemic form. Investigat