96996-90-6

Basic information

• Product Name: 1,2,3,4,6-PENTA-O-BENZOYL-D-MANNOPYRANOSE
• Synonyms: 1,2,3,4,6-PENTA-O-BENZOYL-D-MANNOPYRANOSE;1,2,3,4,6-Pentabenzoate D-Mannopyranose;D-Mannose Pentabenzoate;(3S,4S,5R,6R)-6-((benzoyloxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetrabenzoate;(3S,4S,5R,6R)-6-((benzoyloxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetrabenzoate(WXC02200)
• CAS NO: 96996-90-6
• Molecular Formula: C₄₁H₃₂O₁₁
• Molecular Weight: 700.69
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 96996-90-6.mol
• Article Data: 87

Chemical Properties

• Melting Point: 152-153°C
• Boiling Point: 803.7±65.0 °C(Predicted)
• Appearance: /
• Density: 1.37±0.1 g/cm3(Predicted)
• Storage Temp.: -20°C Freezer
• Solubility: Acetontrile (Slightly), Chloroform (Slightly), Ethyl Acetate (Slightly)
• CAS DataBase Reference: 1,2,3,4,6-PENTA-O-BENZOYL-D-MANNOPYRANOSE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4,6-PENTA-O-BENZOYL-D-MANNOPYRANOSE(96996-90-6)
• EPA Substance Registry System: 1,2,3,4,6-PENTA-O-BENZOYL-D-MANNOPYRANOSE(96996-90-6)

Safety Data

• Hazardous Substances Data: 96996-90-6(Hazardous Substances Data)

Usage

Chemical Properties

White Crystalline Solid

Uses

1,2,3,4,6-Penta-O-benzoyl-D-mannopyranose (cas# 96996-90-6) is a compound useful in organic synthesis.

Upstream product

• 6605-40-9 methyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside 
• 93-97-0 benzoic acid anhydride 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 31273-58-2 1-(7-hydroxy-2,2-dimethylchroman-6-yl)ethanone 
• 140-10-3 (E)-3-phenylacrylic acid 
• 1615-02-7 3-(4-chlorophenyl)prop-2-enoic acid 
• 555-68-0 (E)-3-Nitrocinnamic acid 
• 14737-89-4 3,4-dimethoxy-trans-cinnamic acid 
• 1552-96-1 p-dimethylaminocinnamic acid 
• 118-93-4 o-hydroxyacetophenone 
• 90-02-8 salicylaldehyde 
• 118-61-6 2-hydroxy-benzoic acid ethyl ester 
• 59-23-4 D-Galactose 
• 98-88-4 benzoyl chloride 

Downstream Products

• 14218-11-2 2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide 
• 15067-04-6 (2R,3R,4S,5R,6R)-2-chloro-6-(benzoyloxymethyl)tetrahydro-2H-pyran-3,4,5-triyl tribenzoate 
• 165877-99-6 2,3,4,6-tetra-O-Bz-β-D-glucopyranosyl bromide 
• 105376-04-3 ethyl 2,3,4,6-tetra-O-benzoyl-1-thio-β-D-glucopyranoside 
• 233674-87-8 2,3,4,6-Tetra-O-benzoyl-β-D-galactopyranosyl S-(2-pyridyl) thiocarbonate 
• 233674-88-9 2,3,4,6-Tetra-O-benzoyl-β-D-galactopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-α-D-mannopyranose 
• 6605-40-9 methyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside 
• 113544-59-5 O²,O³,O⁴,O⁶-Tetrabenzoyl-D-mannose 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-α-D-mannopyranoside 
• 6605-40-9 methyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 1011529-30-8 (2-methyl-5-tert-butylphenyl) 2,3,4,6-tetra-O-benzoyl-1-thio-α-D-mannopyranoside 
• 14726-07-9 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl iodide 
• 64768-20-3 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside 
• 188435-38-3 bromide 2,3,4,6-tetra-O-Bz-α-D-galactopyranosyl bromide 

Relevant articles and documents

Facile and efficient access to C1-aminosugar derivatives under mild conditions

A facile and efficient synthesis of C1-aminosugar derivatives under catalyst-free conditions is described here. In particular, readily available benzoyl glycosyl bromides react smoothly to give a broad scope of C1-aminosugar derivatives in good yields. Th

N-aryl sulfanilamide-N-beta-D-glucopyranose diamide compound and application thereof

The invention belongs to the technical field of medicines, and relates to a preparation method and medical application of an N1-aryl sulfanilamide-N4-beta-D-glucopyranose diamide compound. The compound is shown in a general formula (I), substituent groups are described in the specification, and the compound shown in the general formula (I) and an optical active body, a diastereoisomer and a pharmaceutically acceptable salt thereof are applied to preparation of anti-tumor drugs. Based on pharmacophore characteristics and subcellular localization of CA IX and XII, a selective CA IX and XII inhibitor is designed and synthesized, polyhydroxy high-polarity glucose is selected as a tail end, a classical pharmacophore aryl sulfanilamide fragment of a targeted CAs active center is introduced through a flexible aliphatic chain and a rigid aromatic structure, the overall structure can selectively inhibit catalytic activity of extracellular CA IX and XII, an anti-tumor effect is achieved, and therefore, the compound has a good application prospect.

Synthesis and inhibition of α-glucosidase of methyl glycyrrhetinate glycosides

The synthesis of the methyl glycyrrhetinate glycosides and inhibition of α-glucosidase were studied. The carboxyl group of glycyrrhetinic acid was methylated, and glucose and galactose were introduced into the hydroxyl group to obtain compounds 7 and 12.