7464-56-4

Basic information

• Product Name: ALLYL A-D-GLUCOPYRANOSIDE
• Synonyms: ALLYL A-D-GLUCOPYRANOSIDE;ALLYL ALPHA-D-GLUCOPYRANOSIDE;Allyl α-D-Glucopyranoside;2-Propen-1-yl-alpha-D-glucopyranoside;2-Propenyl-alpha-D-glucoside;1-O-allyl-α-D-glucopyranoside
• CAS NO: 7464-56-4
• Molecular Formula: C₉H₁₆O₆
• Molecular Weight: 220.22
• EINECS: 1533716-785-6
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 7464-56-4.mol
• Article Data: 76

Chemical Properties

• Melting Point: 138-141°C
• Boiling Point: 415 ºC at 760 mmHg
• Flash Point: 204.8 ºC
• Appearance: white powder
• Density: 1.37 g/cm³
• Vapor Pressure: 1.27E-08mmHg at 25°C
• Refractive Index: 1.549
• Storage Temp.: -20°C Freezer, Under Inert Atmosphere
• Solubility: DMSO (Slightly), Methanol (Slightly), Water (Slightly)
• PKA: 13.01±0.70(Predicted)
• CAS DataBase Reference: ALLYL A-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYL A-D-GLUCOPYRANOSIDE(7464-56-4)
• EPA Substance Registry System: ALLYL A-D-GLUCOPYRANOSIDE(7464-56-4)

Safety Data

• Hazardous Substances Data: 7464-56-4(Hazardous Substances Data)

Usage

Chemical Properties

Ficin froM Fig Tree Latex is Off-White Crystalline Solid

Uses

Ficin froM Fig Tree Latex is a useful synthetic intermediate for oligosaccharide synthesis

InChI:InChI=1/C9H16O6/c1-2-3-14-9-8(13)7(12)6(11)5(4-10)15-9/h2,5-13H,1,3-4H2

Upstream product

• 50-99-7 D-glucose 
• 107-18-6 allyl alcohol 
• 2280-44-6 D-Glucose 
• 591-87-7 Allyl acetate 
• 604-69-3 β-D-glucose pentaacetate 
• 34272-03-2 propargyl β-D-glucopyranoside 
• 106-95-6 allyl bromide 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 6919-96-6 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 13035-49-9 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl iodide 
• 10343-15-4 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-allyloxy-tetrahydro-pyran-4-yl ester 
• 107-05-1 3-chloroprop-1-ene 
• 93382-48-0 allyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 492-62-6 alpha-D-glucopyranose 

Downstream Products

• 20746-64-9 allyl (R)-4,6-O-benzylidene-β-D-gluco-pyranoside 
• 84276-56-2 allyl 4,6-O-benzylidene-β-D-glucopyranoside 
• 20746-64-9 (2S,4aR,7R,8R,8aR)-6-Allyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 107242-80-8 1-O-allyl-6-O-trityl-α-D-glucopyranoside 
• 65987-12-4 1-O-allyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 6207-45-0 2-allyloxy-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran 
• 83921-82-8 allyl 2,4,6-tri-O-benzyl-α-D-glucopyranoside 
• 83921-79-3 allyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside 
• 6207-44-9 1-allyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 84218-69-9 allyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 146773-64-0 allyl 2,4,6-tri-O-benzyl-β-D-glucopyranoside 
• 225376-17-0 1-O-allyl-6-O-trityl-β-D-glucopyranoside 
• 169822-03-1 allyl 2,6-di-O-benzyl-α-D-glucopyranoside 
• 63976-06-7 1,2,3,4,6-penta-O-allyl-β-D-glucopyranose 

Relevant articles and documents

Anomeric alkylations and acylations of unprotected mono- and disaccharides mediated by pyridoneimine in aqueous solutions

A site-specific deprotonation followed by alkylations and acylations of sugar hemiacetals to the corresponding alkyl glycosides and acylated sugars in aqueous solutions is disclosed herein. Pyridoneimine as a new base is developed to mediate the deprotonation of readily available sugar hemiacetals and further reactions with alkylation and acylation agents.

Carbon tetrachloride-free allylic halogenation-mediated glycosylations of allyl glycosides

The allylic bromination of allyl glycosides is conducted using NBS/AIBN reagents in (EtO)2CO and PhCF3 solutions, without using CCl4 as a solvent. The activated mixed halo-allyl glycosides led to glycosylations, mediated by a triflate, in a latent-active

Synthesis, Conformational Analysis, and Complexation Study of an Iminosugar-Aza-Crown, a Sweet Chiral Cyclam Analog

A new family of chiral C2 symmetric tetraazamacrocycles, coined ISAC for IminoSugar Aza-Crown, incorporating two iminosugars adopting a 4C1 conformation is disclosed. Multinuclear NMR experiments on the corresponding Cdsu