868754-94-3

Basic information

• Product Name: 6-(9H-fluoren-9-ylmethoxycarbonylamino)-hept-3-enedioic acid 7-benzyl ester 1-tert-butyl ester
• Synonyms: 6-(9H-fluoren-9-ylmethoxycarbonylamino)-hept-3-enedioic acid 7-benzyl ester 1-tert-butyl ester
• CAS NO: 868754-94-3
• Molecular Weight: 541.644
• Mol File: 868754-94-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-(9H-fluoren-9-ylmethoxycarbonylamino)-hept-3-enedioic acid 7-benzyl ester 1-tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(9H-fluoren-9-ylmethoxycarbonylamino)-hept-3-enedioic acid 7-benzyl ester 1-tert-butyl ester(868754-94-3)
• EPA Substance Registry System: 6-(9H-fluoren-9-ylmethoxycarbonylamino)-hept-3-enedioic acid 7-benzyl ester 1-tert-butyl ester(868754-94-3)

Safety Data

• Hazardous Substances Data: 868754-94-3(Hazardous Substances Data)

Upstream product

• 146549-21-5 2-(9H-fluoren-9-ylmethoxycarbonylamino)-pent-4-enoic acid 
• 100-39-0 benzyl bromide 
• 14036-55-6 t-butyl vinylacetate 
• 477578-53-3 benzyl (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)pent-4-enoate 

Relevant articles and documents

Convenient access to glutamic acid side chain homologues compatible with solid phase peptide synthesis

(Chemical Equation Presented) Preparation of several side chain length variants of glutamic acid is achieved via olefin cross metathesis of allyl glycine derivatives. The products are suitably protected for direct use in Fmoc solid-phase peptide synthesis, as demonstrated by successful synthesis of test sequences.