82911-76-0

Basic information

• Product Name: N-(9-fluorenylmethyloxycarbonyl)-L-threonine*DCHA
• Synonyms: N-(9-fluorenylmethyloxycarbonyl)-L-threonine*DCHA
• CAS NO: 82911-76-0
• Molecular Weight: 522.685
• Mol File: 82911-76-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(9-fluorenylmethyloxycarbonyl)-L-threonine*DCHA(CAS DataBase Reference)
• NIST Chemistry Reference: N-(9-fluorenylmethyloxycarbonyl)-L-threonine*DCHA(82911-76-0)
• EPA Substance Registry System: N-(9-fluorenylmethyloxycarbonyl)-L-threonine*DCHA(82911-76-0)

Safety Data

• Hazardous Substances Data: 82911-76-0(Hazardous Substances Data)

Upstream product

• 73731-37-0 Fmoc-Thr-OH 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 24324-17-2 9-Fluorenylmethanol 
• 82911-69-1 N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide 
• 82911-72-6 dicyclohexylamine salt of N-hydroxysuccinimide 

Downstream Products

• 120791-80-2 N-(9-Fluorenylmethoxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-azido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonin-tert-butylester 
• 120924-98-3 N-(9-Fluorenylmethoxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-azido-4,6-di-O-benzoyl-2-desoxy-β-D-galactopyranosyl)>-L-threonin-tert-butylester 
• 120792-33-8 N-(9-Fluorenylmethoxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonin-tert-butylester 
• 120791-76-6 N-fluorenylmethoxycarbonyl-threonine-tert-butyl ester 
• 116783-35-8 N-(9H-fluoren-9-yl)methoxycarbonyl-O-(3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-galactopyranosyl)-L-threonine 

Relevant articles and documents

Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxyamino acids using succinimidyl carbonates

9-Fluorenylmethyl succinimidyl, pentachlorophenyl, and benzotriazole-1-yl carbonates were prepared and their reactivity with L-serine and L-serine benzyl ester was compared.The most efficient reagent, 9-fluorenylmethyl succinimidyl carbonate, was used for the preparation of 9-flourenylmethyloxycarbonyl derivatives of other hydroxyamino acids and hydroxyamino acid esters in high yields.The use of trichloroethyl and benzyl succinimidyl carbonates for an efficient conversion of hydroxyamino acids and their esters into the corresponding N-trichloroethoxycarbonyl and benzyloxycarbonyl derivatives is described.