CAS 4435-05-6

Fórmula: C15H22O10

InChI: InChI=1S/C15H22O10/c1-7(16)20-6-10-11(21-8(2)17)12(22-9(3)18)13-14(23-10)25-15(4,19-5)24-13/h10-14H,6H2,1-5H3/t10-,11-,12+,13+,14+,15?/m1/s1

Clave InChI: AUVGRVGPAIFPSA-PEONVUOVSA-N

SMILES: CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]2[C@@H](O1)OC(O2)(C)OC)OC(=O)C)OC(=O)C

(3aS,5R,6R,7S,7aS)-5-(Acetoxymethyl)-2-Methoxy-2-Methyltetrahydro-5H-[1,3]Dioxolo[4,5-b]Pyran-6,7-Diyl Diacetate

CAS: 4435-05-6

Fórmula: C₁₅H₂₂O₁₀

Pureza: 95%

Forma y color: Solid

Peso molecular: 362.3292

Ref: IN-DA00DF96

3,4,6-Tri-O-acetyl-β-D-mannopyranose 1,2-methyl orthoacetate

CAS: 4435-05-6

3,4,6-Tri-O-acetyl-β-D-mannopyranose 1,2-(methyl orthoacetate) is a biochemical reagent utilized in glycobiology research. This field examines the structure, synthesis, biology, and evolution of sugars, involving carbohydrate chemistry, glycoconjugate formation and degradation enzymology, protein-glycan interactions, and the roles of glycans in biological systems. It is closely linked to fundamental research, biomedicine, and biotechnology.

Fórmula: C₁₅H₂₂O₁₀

Peso molecular: 362.33

Ref: TM-TSW-00363

3,4,6-Tri-O-acetyl-Beta-D-mannopyranose 1,2-(Methyl Orthoacetate)

CAS: 4435-05-6

Applications A stable, crystalline precursor for the preparation of acetobromomannose.
References Schroter, S., et al.: J. Biol. Chem., 274, 29862 (1999), Xue, J., et al.: Bioorg. Med. Chem. Lett., 12, 2015 (2002), Schofield, L., et al.: Nature, 418, 785 (2002),

Fórmula: C₁₅H₂₂O₁₀

Forma y color: Neat

Peso molecular: 362.34

Ref: TR-T767000

3,4,6-Tri-O-acetyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose

CAS: 4435-05-6

3,4,6-Tri-O-acetyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose

Fórmula: C₁₄H₂₀O₁₀

Pureza: 95%

Forma y color: Solid

Peso molecular: 348.30259

Ref: 54-BICL4374

3,4,6-Tri-O-acetyl-β-D-mannopyranose 1,2-(methyl orthoacetate)

CAS: 4435-05-6

Peso molecular: 362.33

Ref: 7W-GC8639

3,4,6-Tri-O-acetyl-b-D-mannopyranose 1,2-(methyl orthoacetate)

CAS: 4435-05-6

3,4,6-Tri-O-acetyl-b-D-mannopyranose 1,2-(methyl orthoacetate) is a glycosylation product that is used in the synthesis of oligosaccharides. 3,4,6-Tri-O-acetyl-b-D-mannopyranose 1,2-(methyl orthoacetate) is synthesized by the reaction of 3,4,6-triacetyl b D mannopyranose with methyl orthoacetate in aqueous solution containing an acid catalyst. This compound can be used to modify saccharides and complex carbohydrates. It is also used in click chemistry to create modified sugars. The molecular weight of this compound ranges from 200 to 600 grams per mole and it has a CAS number of 4435 05 6.

Fórmula: C₁₅H₂₂O₁₀

Pureza: Min. 95%

Forma y color: Powder

Peso molecular: 362.33 g/mol

Ref: 3D-MT04874