CAS 4435-05-6

Formel: C15H22O10

InChl: 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

InChI Key: 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

3,4,6-Tri-O-acetyl-b-D-mannopyranose1,2-(methylorthoacetate)

CAS: 4435-05-6

Formel: C₁₅H₂₂O₁₀

Reinheit: 95%

Farbe und Form: Solid

Molekulargewicht: 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.

Formel: C₁₅H₂₂O₁₀

Molekulargewicht: 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),

Formel: C₁₅H₂₂O₁₀

Farbe und Form: Neat

Molekulargewicht: 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

Formel: C₁₄H₂₀O₁₀

Reinheit: 95%

Farbe und Form: Solid

Molekulargewicht: 348.30259

Ref: 54-BICL4374

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

CAS: 4435-05-6

Molekulargewicht: 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.

Formel: C₁₅H₂₂O₁₀

Reinheit: Min. 95%

Farbe und Form: Powder

Molekulargewicht: 362.33 g/mol

Ref: 3D-MT04874