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Home CSCS20620708813

(3aS,4R,6S,6aS)-4-[(1R)-1,2-dihydroxyethyl]-6-hydroxy-tetrahydro-2H-furo[3,4-d][1,3]dioxol-2-one

Structure Info

Chemspace ID
CSCS20620708813 (Synthesis)
IUPAC Name
(3aS,4R,6S,6aS)-4-[(1R)-1,2-dihydroxyethyl]-6-hydroxy-tetrahydro-2H-furo[3,4-d][1,3]dioxol-2-one
Mol formula
C7H10O7
Mol weight
206 Da
Catalog Number(s)
HY-W411889, TSW-00392

Properties

LogP
-1.35
Heavy atoms count
14
Rotatable bond count
2
Number of rings
2
Carbon bond saturation, Fsp3
0.857
Polar surface area (Å)
105
Hydrogen bond acceptors count
6
Hydrogen bond donors count
3

SDS

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C7H10O7
Zoom the structure
CSCS20620708813
 

Items Overall 3 items from 3 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
MedChemExpressTBDUnited States
To:
901 mgPOA
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Description: Names: α-D-Mannofuranose, cyclic 2,3-carbonate; Product Description: α-D-Mannofuranose, cyclic 2,3-carbonate 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; Target: Biochemical Assay Reagents; CAS: 76548-27-1
MedChemExpress EUTBDSweden
To:
901 mgPOA
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Description: Names: α-D-Mannofuranose, cyclic 2,3-carbonate; Product Description: α-D-Mannofuranose, cyclic 2,3-carbonate 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; Target: Biochemical Assay Reagents; CAS: 76548-27-1
Targetmol Chemicals IncTBDUnited States
To:
901 mgPOA
Go to cartEnquire
Description: α-D-Mannofuranose, cyclic 2,3-carbonate is a biochemical reagent utilized in glycoscience research. Glycoscience explores the structure, synthesis, biology, and evolution of sugars. It encompasses carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.; CAS: 76548-27-1
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