CAS 3082-96-0
:Methyl D-glucopyranuronate 1,2,3,4-tetraacetate
Description:
Methyl D-glucopyranuronate 1,2,3,4-tetraacetate is a chemical compound characterized by its structure, which includes a glucopyranose ring modified with four acetyl groups and a methyl ester functional group. This compound is a derivative of D-glucuronic acid, featuring a pyranose form that contributes to its cyclic structure. The presence of multiple acetyl groups enhances its solubility in organic solvents and can influence its reactivity and biological activity. Methyl D-glucopyranuronate tetraacetate is typically used in biochemical applications, including as a substrate in enzymatic reactions or as a building block in the synthesis of more complex molecules. Its CAS number, 3082-96-0, allows for easy identification in chemical databases. The compound is generally stable under standard laboratory conditions, but like many acetylated compounds, it may be sensitive to hydrolysis in the presence of moisture or strong bases. Overall, its unique structural features make it a valuable compound in organic synthesis and biochemical research.
Formula:C15H20O11
InChI:InChI=1S/C15H20O11/c1-6(16)22-10-11(23-7(2)17)13(24-8(3)18)15(25-9(4)19)26-12(10)14(20)21-5/h10-13,15H,1-5H3/t10-,11-,12-,13+,15?/m0/s1
InChI key:InChIKey=DPOQCELSZBSZGX-BVIXPPBVSA-N
SMILES:O(C(C)=O)[C@H]1[C@H](OC(C)=O)[C@@H](C(OC)=O)OC(OC(C)=O)[C@@H]1OC(C)=O
Synonyms:- <span class="text-smallcaps">D</span>-Glucopyranuronic acid, methyl ester, 1,2,3,4-tetraacetate
- <span class="text-smallcaps">D</span>-Glucopyranuronic acid, methyl ester, tetraacetate
- D-Glucopyranuronicacid, methyl ester, tetraacetate (9CI)
- Glucopyranuronic acid, methyl ester, tetraacetate
- Glucopyranuronic acid, methyl ester, tetraacetate, <span class="text-smallcaps">D</span>-
- Glucopyranuronic acid, methyl ester, tetraacetate, D-(8CI)
- Glucopyranuronic acid, methyl ester,tetraacetate (6CI,7CI)
- Methyl 1,2,3,4-tetra-O-acetyl-α/β-D-glucopyranouronate
- Methyl <span class="text-smallcaps">D</span>-glucopyranuronate 1,2,3,4-tetraacetate
- D-Glucopyranuronic acid, methyl ester, tetraacetate
- Glucopyranuronic acid, methyl ester, tetraacetate, D-
- D-Glucopyranuronic acid, methyl ester, 1,2,3,4-tetraacetate
- See more synonyms
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Found 6 products.
1,2,3,4-TETRA-O-ACETYL-D-GLUCOPYRANURONIC ACID METHYL ESTER
CAS:Formula:C15H20O11Purity:97%Color and Shape:SolidMolecular weight:376.3127Methyl 1,2,3,4-tetra-O-acetyl-D-glucopyranuronate
CAS:<p>Methyl 1,2,3,4-tetra-O-acetyl-D-glucopyranuronate</p>Purity:97%(3R,4S,5S,6S)-6-(METHOXYCARBONYL)TETRAHYDRO-2H-PYRAN-2,3,4,5-TETRAYL TETRAACETATE
CAS:Formula:C15H20O11Purity:97%Molecular weight:376.3141,2,3,4-Tetra-O-acetyl-α,β-D-glucuronic Acid, Methyl Ester (mixture of anomers)
CAS:Controlled Product<p>Applications 1,2,3,4-Tetra-O-acetyl-α,β-D-glucuronic Acid, Methyl Ester _x000D_(mixture of anomers) (cas# 3082-96-0) is a compound useful in organic synthesis.<br></p>Formula:C15H20O11Color and Shape:NeatMolecular weight:376.311,2,3,4-Tetra-O-acetyl-D-glucuronide methyl ester
CAS:<p>1,2,3,4-Tetra-O-acetyl-D-glucuronide methyl ester is a lactone that can be used as a precursor for the synthesis of various types of compounds. The chemical structure was determined by high-resolution x-ray diffraction to be a planar molecule with two conformations: one where the four acetyl groups are on different sides and another where they are all on the same side. The latter conformation is more stable due to the dihedral angle between the hydroxyl group and carbonyl group. This compound is an intermediate in synthesizing 2-(4'-hydroxybenzoyl)-1,2,3,4-tetra-O-acetyl-.alpha.-D-.beta.-D glucopyranoside methyl ester by reacting with 3-(3'-azido)benzaldehyde. The single crystal x-ray diffraction study revealed that this compound has a conformation</p>Formula:C15H20O11Purity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:376.31 g/mol






