| Identification | Back Directory | [Name]
.alpha.-D-Glucopyranoside, phenyl 1-thio-, tetraacetate | [CAS]
13992-16-0 | [Synonyms]
phenyl 2,3,4,6-tetra-O-acetyl-α-D-1-thio-Mannoside
phenyl 2,3,4,6-tetra-O-acetyl-α-D-1-thio-Mannoside
Phenyl 2,3,4,6-tetra-O-acetyl-α-D-thiomannopyranoside
.alpha.-D-Glucopyranoside, phenyl 1-thio-, tetraacetate
Phenyl 1-thio-alpha-D-glucopyranoside 2,3,4,6-tetraacetate
(3,4,5-Triacetyloxy-6-phenylsulfanyloxan-2-yl)methyl acetate
Phenyl 2,3,4,6-tetra-O-acetyl-alpha-D-thiomannopyranoside 97%
(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(phenylthio)tetrahydro-2H-pyran-3,4,5-triyl triacetate | [Molecular Formula]
C20H24O9S | [MDL Number]
MFCD01862644 | [MOL File]
13992-16-0.mol | [Molecular Weight]
440.46 |
| Chemical Properties | Back Directory | [Melting point ]
85-87°C | [Boiling point ]
514.6±50.0 °C(Predicted) | [density ]
1.31±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [form ]
solid | [InChI]
InChI=1/C20H24O9S/c1-11(21)25-17-16(10-15-8-6-5-7-9-15)28-20(30-29-14(4)24)19(27-13(3)23)18(17)26-12(2)22/h5-9,16-20H,10H2,1-4H3/t16-,17-,18+,19-,20-/s3 | [InChIKey]
XGVRJQXCDRSLIC-SKAYCTISNA-N | [SMILES]
S(OC(=O)C)[C@H]1O[C@H](CC2=CC=CC=C2)[C@@H](OC(=O)C)[C@H](OC(=O)C)[C@H]1OC(=O)C |&1:5,7,15,20,25,r| |
| Hazard Information | Back Directory | [Uses]
Phenyl 2,3,4,6-tetra-O-acetyl-α-D-thiomannopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1]. | [References]
[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922 |
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