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30854-62-7, Hepta-O-acetyl-b-lactosyl azide, CAS:30854-62-7

30854-62-7, Hepta-O-acetyl-b-lactosyl azide, CAS:30854-62-7
C26H35N3O17 / 661.57
MFCD05664728

七乙酰基-1-脱氧-1-叠氮-beta-D-乳糖,    2,3,6,2',3',4',6'-Hepta-O-acetyl-b-lactosyl azide

2,3,6,2',3',4',6'-Hepta-O-acetyl-b-lactosyl azide is a custom synthesis of a carbohydrate that has been modified by the addition of acetyl groups to one end and the attachment of an azide group to the other. The synthesis of this compound has been completed in high purity and is available for purchase. This compound is a complex carbohydrate that is a sugar that can be modified by fluorination. It is also an oligosaccharide or polysaccharide with saccharide units.

CAS Number30854-62-7
Product Name[(2R,3R,4S,5R,6R)-4,5-diacetyloxy-6-azido-3-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate
IUPAC Name[(2R,3R,4S,5R,6R)-4,5-diacetyloxy-6-azido-3-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate
Molecular FormulaC26H35N3O17
Molecular Weight661.57 g/mol
InChIInChI=1S/C26H35N3O17/c1-10(30)37-8-17-20(21(40-13(4)33)23(42-15(6)35)25(44-17)28-29-27)46-26-24(43-16(7)36)22(41-14(5)34)19(39-12(3)32)18(45-26)9-38-11(2)31/h17-26H,8-9H2,1-7H3/t17-,18-,19-,20-,21+,22+,23-,24-,25-,26+/m1/s1
InChI KeyJFCQZWVIHHPJTD-SVRUBWSYSA-N
SMILESCC(=O)OCC1C(C(C(C(O1)N=[N+]=[N-])OC(=O)C)OC(=O)C)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
Canonical SMILESCC(=O)OCC1C(C(C(C(O1)N=[N+]=[N-])OC(=O)C)OC(=O)C)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILESCC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)N=[N+]=[N-])OC(=O)C)OC(=O)C)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C


CAS No: 30854-62-7 Synonyms: b-Lactosyl azide heptaacetate2,3,6-Tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-b-D-galactopyranosyl)-b-D-glucopyranosyl azide MDL No: MFCD05664728 Chemical Formula: C26H35N3O17 Molecular Weight: 661.57
References: 1. Blanco JLJ, Barria CS, Benito JM, Mellet CO, Fuentes J, Santoyo-González F, Femández JMG, Synthesis 1999, No11, p1907-1914


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