100929-05-3

Basic information

• Product Name: 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-benzylester
• Synonyms: 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-benzylester
• CAS NO: 100929-05-3
• Molecular Weight: 1173.19
• Mol File: 100929-05-3.mol

Chemical Properties

• CAS DataBase Reference: 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-benzylester(CAS DataBase Reference)
• NIST Chemistry Reference: 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-benzylester(100929-05-3)
• EPA Substance Registry System: 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-benzylester(100929-05-3)

Safety Data

• Hazardous Substances Data: 100929-05-3(Hazardous Substances Data)

Upstream product

• 87376-57-6 2-azido-4,6-di-O-benzoyl-2-deoxy-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-galactopyranosyl bromide 
• 73724-48-8 N-(fluoren-9-ylmethoxycarbonyl)-L-threonine benzyl ester 
• 108-24-7 acetic anhydride 
• 100929-02-0 N-(9-Fluorenylmethoxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-azido-4,6-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonin-benzylester 

Downstream Products

• 101376-32-3 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 
• 100929-08-6 C₄₇H₅₄N₂O₁₉ 

Relevant articles and documents

Synthesis of glycopeptides with the TN and T antigen structures, and their coupling to bovine serum albumin.

Glycopeptides with TN and T antigen structures that represent the N-terminal tripeptide of asialoglycophorin with blood-group M specificity have been synthesized using fluorenylmethoxycarbonyl (Fmoc) and 2-pyridylethoxycarbonyl (Pyoc) groups for amino pro

Building Units of Oligosaccharides, LXXIII. - Synthesis of the Tetrapeptide Sequence 12 to 15 of Asialoglycophorin A with Four Disaccharide Side Chains

The protected O-glycosylated derivative of L-serine 2 and the homologous L-threonine compound 8, both with the Fmoc-group at the N-terminus and the benzyl ester at the C-terminus, can be used successfully in the synthesis of O-glycopeptides.In these compo