657395-98-7

Basic information

• Product Name: Fmoc-L-Thr(β-D-Lac(Ac)7)-OH
• Synonyms: Fmoc-L-Thr(β-D-Lac(Ac)7)-OH;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-O-[2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyl)-beta-D-glucopyranosyl]-L-threonine;Hepta-O-acetyl-b-Lactosyl-N-Fmoc-L-threonine
• CAS NO: 657395-98-7
• Molecular Formula: C45H53NO22
• Molecular Weight: 959.89582
• EINECS: -0
• Mol File: 657395-98-7.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Fmoc-L-Thr(β-D-Lac(Ac)7)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: Fmoc-L-Thr(β-D-Lac(Ac)7)-OH(657395-98-7)
• EPA Substance Registry System: Fmoc-L-Thr(β-D-Lac(Ac)7)-OH(657395-98-7)

Safety Data

• Hazardous Substances Data: 657395-98-7(Hazardous Substances Data)

Upstream product

• 18464-08-9 4’-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2’,3’,6’-tri-O-acetyl-D-glucopyranose 
• 73724-48-8 N-(fluoren-9-ylmethoxycarbonyl)-L-threonine benzyl ester 
• 92052-38-5 2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-lactosyl trichloroacetimidate 
• 66073-13-0 α-D-glucopyranose-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,6-triacetate 
• 92052-38-5 4-O-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl trichloracetimidate 
• 18464-08-9 4’-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2’,3’,6’-tri-O-acetyl-D-glucopyranose 
• 92052-38-5 1-alpha-trichloroacetimidoyl-2,3,6-O-triacetylglucopyranosyl-4-alpha-(2′,3′,4',6'-O-tetraacetyl)glucopyranoside 
• 73731-37-0 Fmoc-Thr-OH 
• 3616-19-1 1',2',3',6',2,3,4,6-octa-O-acetyl-β-D-lactose 
• 20764-63-0 β-cellobioseoctaacetate 

Relevant articles and documents

Effect of distal sugar and interglycosidic linkage of disaccharides on the activity of proline rich antimicrobial glycopeptides

The effect of glycosylation on protein structure and function depends on a variety of intrinsic factors including glycan chain length. We have analyzed the effect of distal sugar and interglycosidic linkage of disaccharides on the properties of proline-ri

Facile synthesis of glycosylated Fmoc amino acid building blocks assisted by microwave irradiation

The synthesis of glycosylated Fmoc amino acids by reaction of mono- and disaccharide peracetates with Fmoc amino acids having free carboxyl groups was rapidly promoted by Lewis acids (SnCl4, BF3·Et 2O) under microwave irradiation. The products are useful building blocks for the synthesis of glycopeptides.