CAS 6564-72-3
:2,3,4,6-Tetrakis-O-(phenylmethyl)-α-D-glucopyranose
Description:
2,3,4,6-Tetrakis-O-(phenylmethyl)-α-D-glucopyranose is a glycoside derivative of glucose, characterized by the presence of four phenylmethyl (benzyl) groups attached to the hydroxyl positions of the glucopyranose ring. This compound is typically a white to off-white crystalline solid, exhibiting good solubility in organic solvents such as methanol and ethanol, while being less soluble in water due to its bulky phenylmethyl substituents. The presence of these substituents enhances its lipophilicity and may influence its biological activity, making it of interest in various fields, including medicinal chemistry and carbohydrate chemistry. The compound can undergo hydrolysis under acidic or enzymatic conditions, releasing the parent glucose molecule. Its structure allows for potential applications in drug delivery systems, as the phenylmethyl groups can facilitate interactions with biological membranes. Additionally, the compound's stereochemistry and functional groups contribute to its reactivity and potential interactions with other chemical entities. Overall, 2,3,4,6-Tetrakis-O-(phenylmethyl)-α-D-glucopyranose is a versatile compound with significant implications in research and development.
Formula:C34H36O6
InChI:InChI=1/C34H36O6/c35-34-33(39-24-29-19-11-4-12-20-29)32(38-23-28-17-9-3-10-18-28)31(37-22-27-15-7-2-8-16-27)30(40-34)25-36-21-26-13-5-1-6-14-26/h1-20,30-35H,21-25H2/t30-,31-,32+,33-,34?/m1/s1
InChI key:InChIKey=OGOMAWHSXRDAKZ-RUOAZZEASA-N
SMILES:O(CC1=CC=CC=C1)[C@H]2[C@H](OCC3=CC=CC=C3)[C@@H](COCC4=CC=CC=C4)O[C@H](O)[C@@H]2OCC5=CC=CC=C5
Synonyms:- (2S,3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-ol
- 2, 3, 4, 6-Tetra-O-Benzyl-α-<span class="text-smallcaps">D</span>-glucopyranose
- 2,3,4,6-Tetra-O-benzyl-D-glucofuranose
- 2,3,4,6-Tetra-O-benzyl-alpha-D-glucose
- 2,3,4,6-Tetra-O-benzyl-α-<span class="text-smallcaps">D</span>-glucopyranose
- 2,3,4,6-Tetra-O-benzyl-α-<span class="text-smallcaps">D</span>-glucose
- 2,3,4,6-Tetrakis-O-(phenylmethyl)-α-<span class="text-smallcaps">D</span>-glucopyranose
- Glucopyranose, 2,3,4,6-tetra-O-benzyl-, α-<span class="text-smallcaps">D</span>-
- α-<span class="text-smallcaps">D</span>-Glucopyranose, 2,3,4,6-tetrakis-O-(phenylmethyl)-
- Glucopyranose, 2,3,4,6-tetra-O-benzyl-, α-D-
- 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranose
- α-D-Glucopyranose, 2,3,4,6-tetrakis-O-(phenylmethyl)-
- 2, 3, 4, 6-Tetra-O-Benzyl-α-D-glucopyranose
- 2,3,4,6-Tetrakis-O-(phenylmethyl)-α-D-glucopyranose
- 2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSIDE
- 2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSE
- 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranos
- 2,3,4,6-TETRA-O-ACETYL A-D-GLUCOPYRANOSIDE
- 2,3,4,6-Tetra-o-benzyl-D-glucopyransoe
- 2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSE ,GB
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Found 6 products.
2,3,4,6-Tetra-O-benzyl-α-D-glucopyranose, 98%
CAS:<p>It is the intermediate of Voglibose/Dapagliflozin. An important D-glucopyranose derivative for glucosylations and other reactions 1,2; Preparation of the -glucopyranosyl chloride, synthesis of 1-C--D-glucopyranose derivatives. This Thermo Scientific Chemicals brand product was originally part of the</p>Formula:C34H36O6Purity:98%Color and Shape:White to pale cream, Crystals or powder or crystalline powderMolecular weight:540.662,3,4,6-Tetra-O-benzyl-α-D-glucopyranose
CAS:Formula:C34H36O6Purity:97%Color and Shape:SolidMolecular weight:540.64602,3,4,6-Tetra-O-Benzyl-D-Glucopyranose
CAS:<p>2,3,4,6-Tetra-O-Benzyl-D-Glucopyranose</p>Purity:97%Molecular weight:540.65g/mol(2S,3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-ol
CAS:Purity:98%Color and Shape:SolidMolecular weight:540.65600592,3,4,6-Tetra-O-benzyl-a-D-glucopyranose
CAS:<p>2,3,4,6-Tetra-O-benzyl-a-D-glucopyranose is a synthetic derivative of galactose that can be used as a sugar donor in the synthesis of various types of glycosides. It is activated with phosphorus oxychloride and aluminium chloride to yield the corresponding anhydride. The hydroxy group on 2,3,4,6-tetra-O-benzyl-a-D-glucopyranose may be converted to an alkene by condensation with naphthalene or another electrophile. The stereoselective introduction of the hydroxy group using this method provides a valuable tool for chemists who are interested in synthesizing chiral molecules.</p>Formula:C34H36O6Purity:Min. 95%Color and Shape:White crystals.Molecular weight:540.65 g/mol





