1386972-45-7

Basic information

• Product Name: 2'-(9H-fluoren-9-yl)methoxycarbonylaminoethyl-3-O-acetyl-2-azido-4-O-benzyl-6-O-(tert-butyldiphenylsilyl)-2-deoxy-α-D-glucopyranoside
• Synonyms: 2'-(9H-fluoren-9-yl)methoxycarbonylaminoethyl-3-O-acetyl-2-azido-4-O-benzyl-6-O-(tert-butyldiphenylsilyl)-2-deoxy-α-D-glucopyranoside
• CAS NO: 1386972-45-7
• Molecular Weight: 841.048
• Mol File: 1386972-45-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2'-(9H-fluoren-9-yl)methoxycarbonylaminoethyl-3-O-acetyl-2-azido-4-O-benzyl-6-O-(tert-butyldiphenylsilyl)-2-deoxy-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-(9H-fluoren-9-yl)methoxycarbonylaminoethyl-3-O-acetyl-2-azido-4-O-benzyl-6-O-(tert-butyldiphenylsilyl)-2-deoxy-α-D-glucopyranoside(1386972-45-7)
• EPA Substance Registry System: 2'-(9H-fluoren-9-yl)methoxycarbonylaminoethyl-3-O-acetyl-2-azido-4-O-benzyl-6-O-(tert-butyldiphenylsilyl)-2-deoxy-α-D-glucopyranoside(1386972-45-7)

Safety Data

• Hazardous Substances Data: 1386972-45-7(Hazardous Substances Data)

Upstream product

• 220645-79-4 p-methylphenyl 2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 31505-45-0 2-deoxy-2-phthalimido-β-D-glucopyranose 
• 172847-90-4 p-methylphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 14131-63-6 D-glucosamine hydrochloride 
• 28920-43-6 (fluorenylmethoxy)carbonyl chloride 
• 1386972-44-6 C₂₂H₂₅N₃O₅S 
• 1383446-30-7 thiotolyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-(tert-butyldiphenylsilyl)-2-deoxy-β-D-glucopyranoside 
• 105496-31-9 N-(9-fluorenylmethoxycarbonyl)-2-aminoethanol 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose 

Downstream Products

• 1386972-49-1 2'-aminoethyl 3-O-acetyl-2-azido-4-O-benzyl-6-O-(tert-butyldiphenylsilyl)-2-deoxy-α-D-glucopyranoside 

Relevant articles and documents

Solid-phase synthesis of 2-aminoethyl glucosamine sulfoforms

Mono- and disaccharides of sulfonated glucosamines (GlcN sulfoforms) conjugated to 2-aminoethyl linkers were generated by solid-phase synthesis. Orthogonally protected intermediates were tethered onto tritylated polystyrene resin beads, subjected to amodular sequence of deprotection and sulfonation steps, then cleaved from solid support without degradation of N- or O-sulfate esters using solvolytic conditions, and finally purified by reverse-phase HPLC to afford the title compounds. Copyright Taylor & Francis Group, LLC.