83476-52-2

Basic information

• Product Name: propargyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
• Synonyms: propargyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside
• CAS NO: 83476-52-2
• Molecular Weight: 386.356
• Mol File: 83476-52-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: propargyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: propargyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(83476-52-2)
• EPA Substance Registry System: propargyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside(83476-52-2)

Safety Data

• Hazardous Substances Data: 83476-52-2(Hazardous Substances Data)

Upstream product

• 107-19-7 propargyl alcohol 
• 572-10-1 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl chloride 

Downstream Products

• 83476-63-5 Acetic acid (2R,3R,4S,5S,6S)-3,5-diacetoxy-2-acetoxymethyl-6-[2,5-bis-((2S,3S,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxymethyl)-benzyloxy]-tetrahydro-pyran-4-yl ester 
• 287967-77-5 Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{4-[3-((2S,3S,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenoxy}-tetrahydro-pyran-3-yl ester 
• 1194524-97-4 3-[3,3'''-didodecyl-5'''-[3-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyloxy)-1-propyn-1-yl][2,2':5',2'':5'',2'''-quaterthien]-5-yl]-2-propyn-1-yl-α-D-mannopyranose tetraacetate 
• 287967-83-3 Acetic acid (2R,3R,4S,5S,6S)-3,5-diacetoxy-2-acetoxymethyl-6-(3-{4-[3-((2S,3S,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-prop-2-ynyloxy)-tetrahydro-pyran-4-yl ester 
• 83476-72-6 C₅₁H₆₆O₃₀ 
• 400783-42-8 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetrakis{4'-[1''-O-(α-D-mannopyranosyl)prop-3''-ynyl]benzyloxy}calix[4]arene 
• 400783-41-7 25,26,27,28-tetrakis{4'-[1''-(α-D-mannopyranosyl)prop-3''-ynyl]benzyloxy}calix[4]arene 

Relevant articles and documents

Expedient and facile one-pot syntheses of triazole-linked glycoconjugates under microwave irradiation

Effective microwave assisted one-pot syntheses of triazole-O- glycoconjugates and triazolylglycosides involving sequential glycosylation and click chemistry are described. Georg Thieme Verlag Stuttgart · New York.