93382-48-0

Basic information

• Product Name: allyl 4,6-O-benzylidene-α-D-glucopyranoside
• Synonyms: allyl 4,6-O-benzylidene-α-D-glucopyranoside
• CAS NO: 93382-48-0
• Molecular Weight: 308.331
• Mol File: 93382-48-0.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: allyl 4,6-O-benzylidene-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 4,6-O-benzylidene-α-D-glucopyranoside(93382-48-0)
• EPA Substance Registry System: allyl 4,6-O-benzylidene-α-D-glucopyranoside(93382-48-0)

Safety Data

• Hazardous Substances Data: 93382-48-0(Hazardous Substances Data)

Usage

General Description

Allyl 4,6-O-benzylidene-α-D-glucopyranoside is a chemical compound that is derived from glucose and contains a benzylidene group. It is a colorless, odorless solid at room temperature and is often used as a building block in organic synthesis. allyl 4,6-O-benzylidene-α-D-glucopyranoside has been studied for its potential biological activities, including its antifungal and antibacterial properties, as well as its potential as an anti-inflammatory agent. Additionally, allyl 4,6-O-benzylidene-α-D-glucopyranoside has been investigated for its potential applications in the pharmaceutical and food industries due to its unique chemical properties. Overall, this compound is of interest for its diverse potential applications in various fields.

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 48149-74-2 allyl D-glucopyranoside 
• 2595-07-5 allyl β-D-glucopyranoside 
• 100-52-7 benzaldehyde 
• 2280-44-6 D-Glucose 
• 3006-41-5 4,6-O-benzylidene-α,β-D-galactopyranose 
• 106-95-6 allyl bromide 
• 2595-07-5 allyl D-galactopyranoside 
• 7464-56-4 1-O-allyl-α-D-glucopyranoside 
• 107-18-6 allyl alcohol 
• 492-61-5 β-D-glucose 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 10343-15-4 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-allyloxy-tetrahydro-pyran-4-yl ester 
• 604-69-3 β-D-glucose pentaacetate 

Downstream Products

• 103833-57-4 allyl 4,6-O-benzylidene-2,3-di-O-benzyl-α-D-glucopyranoside 
• 303752-88-7 Allyl 2,3-Bis-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-galactopyranoside 
• 145773-08-6 allyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 130249-97-7 4-Methyl-benzoic acid (2R,4aR,6S,7R,8S,8aS)-6-allyloxy-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 156325-61-0 allyl 4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside 
• 127514-28-7 Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 

Relevant articles and documents

A Synthetic Carbohydrate-Protein Conjugate Vaccine Candidate against Klebsiella pneumoniae Serotype K2

Klebsiella pneumoniae causes pneumonia and liver abscesses in humans worldwide and contains virulence factor capsular polysaccharides and lipopolysaccharides linked to the cell wall. Although capsular polysaccharides are good antigens for vaccine producti

Assembly of a β-(1?→?3)-glucan laminarihexaose on ionic liquid support

An efficient method for the preparation of β-(1?→?3)-D-glucan laminarihexaose on ionic liquid (IL)-support is described. A β-(1?→?3)-glucan laminarihexaose was rapidly assembled in 15?h in a stereoselective fashion with an average yield of over 90% per st

2,4,6-Trichloro-1,3,5-triazine (TCT) mediated one-pot sequential functionalisation of glycosides for the generation of orthogonally protected monosaccharide building blocks

Orthogonally protected monosaccharide building blocks have been prepared using TCT in a one-pot multicomponent transformation. The process involves successive steps of arylidene acetalation, esterification and regioselective reductive acetal cleavage. High regioselectivity, scope for using a broad range of substrates, functional group tolerance, mild reaction conditions, easy handling process and wide application range are a few advantages of the current process.