3006-41-5

Basic information

• Product Name: 4,6-O-BENZYLIDENE-D-GALACTOSE
• Synonyms: 4,6-O-BENZYLIDENE-D-GALACTOSE;4,6-O-Benzylidene-D-galactose ,98%;4,6-O-(Phenylmethylene)-D-galactopyranose
• CAS NO: 3006-41-5
• Molecular Formula: C₁₃H₁₆O₆
• Molecular Weight: 268.26
• EINECS: 1533716-785-6
• Product Categories: Carbohydrates;Carbohydrates A to;Carbohydrates A-CBiochemicals and Reagents;Monosaccharide
• Mol File: 3006-41-5.mol
• Article Data: 40

Chemical Properties

• Boiling Point: 483℃
• Flash Point: 246℃
• Appearance: /
• Density: 1.436
• Storage Temp.: −20°C
• CAS DataBase Reference: 4,6-O-BENZYLIDENE-D-GALACTOSE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-O-BENZYLIDENE-D-GALACTOSE(3006-41-5)
• EPA Substance Registry System: 4,6-O-BENZYLIDENE-D-GALACTOSE(3006-41-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 3006-41-5(Hazardous Substances Data)

Usage

General Description

4,6-O-BENZYLIDENE-D-GALACTOSE is a chemical compound with the molecular formula C13H14O6. It is a derivative of galactose, a type of sugar found in milk and dairy products. The benzylidene group at the 4 and 6 positions of the galactose molecule makes it suitable for various organic synthesis reactions. This chemical is commonly used as a building block in the synthesis of various biologically active compounds and pharmaceuticals. It is also used as a chiral building block in the production of complex carbohydrate derivatives for pharmaceutical and biotechnological applications. Additionally, 4,6-O-BENZYLIDENE-D-GALACTOSE is utilized as a ligand for the development of novel metal-organic frameworks and as a starting material for the preparation of asymmetric catalysts.

Upstream product

• 50-99-7 D-glucose 
• 100-52-7 benzaldehyde 
• 10257-28-0 D-Galactose 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 2280-44-6 D-Glucose 
• 492-62-6 alpha-D-glucopyranose 
• 50-99-7 D-glucose 
• 59-23-4 D-Galactose 
• 113533-74-7 (2R,4aR,7R,8R,8aS)-6-Pent-4-enyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 1269490-06-3 N,O-dimethyl-N-(4,6-O-benzylidene-β-D-glucopyranosyl)hydroxylamine 
• 604-69-3 β-D-glucose pentaacetate 
• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 530-26-7 D-Mannose 

Downstream Products

• 151795-05-0 5,7-O-benzylidene-D-glycero-D-ido-heptono-1,4-lactone 
• 151795-04-9 5,7-O-benzylidene-D-glycero-D-gulo-heptono-1,4-lactone 
• 257925-66-9 acetyl 2,3-di-O-acetyl-4,6-O-benzyliden-D-glucopyranoside 
• 3006-42-6 1,2,3,-tri-O-acetyl-4,6-O-benzylidene-D-galactose 
• 99274-32-5 2,4-O-benzylidene-D-threose 
• 103411-88-7 (2S,4aR,6R,6aS,8S,10aR,12S,12aS)-2,8-Diphenyl-octahydro-1,3,5,7,9,11-hexaoxa-dibenzo[a,e]cyclooctene-6,12-diol 
• 116237-14-0 2,4-O-Benzylidene-3-formyl-D-erythrose 
• 81577-69-7 [2R,4R,5R]-5-hydroxy-2-phenyl-[1,3]dioxane-4-carbaldehyde 
• 76696-05-4 (4aS,6S,8aS)-2-((2R,4R,5R)-5-Hydroxy-2-phenyl-[1,3]dioxan-4-yl)-6-phenyl-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-ol 
• 173936-77-1 1,2,3-tri-O-acetyl-4,6-di-O-benzylidene-β-D-glucopyranose 
• 173936-76-0 1,2,3-tri-O-acetyl-4,6-O-benzylidene-α-D-glucopyranose 
• 175980-93-5 (2S,4aR,6S,7R,8R,8aR)-6-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 60618-81-7 1,2,3-tri-O-acetyl-4,6-O-benzylidene-β-D-glucopyranose 

Relevant articles and documents

An Improved, Versatile, and Easily Scalable Synthesis of Sphingomyelins: Application to Stable Isotope Labeling

With a view to make conveniently labeled mass spectrometry standards available, a set of deuterated sphingomyelins were prepared by a new expedient, flexible, robust, scalable, and high-yielding synthetic scheme starting from 2-azido-3- O -benzoylsphingos

NATURAL AND SYNTHETIC DITERPENE GLYCOSIDES, COMPOSITIONS AND METHODS

Novel diterpene glycosides isolated from Stevia extract as well as diterpene glycosides that are synthetically prepared are provided herein. Compositions and consumables comprising the novel diterpene glycosides are also provided herein. Methods of enhancing the sweetness and/or flavor of consumables using the novel diterpene glycosides, methods of preparing compositions and consumables comprising the novel diterpene glycosides, methods of purifying the novel diterpene glycosides and methods of synthesizing the diterpene glycosides are also provided.

Oligosaccharide compound and its manufacture and its intermediate

The purpose of the present invention is to provide an oligosaccharide with high versatility that can produce a protected sulfate oligosaccharide that can become a manufacturing intermediate of polysulfated hyaluronic acid, and to provide a manufacturing method therefor and an intermediate thereof. Position 2 amino groups in glucosamine, galactosamine, and the like can react with saccharide receptors having an electron attracting group such as glucuronic acid and protected sulfate groups, by using a saccharide donor protected by a specific protective group.