Basic information
- CAS
13299-15-5- Standard SMILES
OC[C@H]1O[C@H](O)C[C@@H](O)[C@@H]1O- InChIKey
PMMURAAUARKVCB-ZXXMMSQZSA-N- Molecular formula
- C6H12O5
- Average molar mass
- 164.16 g/mol
- Monoisotopic mass
- 164.06847348
Overview
(2S,4R,5S,6R)-6-(hydroxymethyl)oxane-2,4,5-triol is a hexose.
Names & identifiers
- Preferred name
- alpha-D-2-Deoxyglucopyranose
- IUPAC
- (2S,4R,5S,6R)-6-(hydroxymethyl)oxane-2,4,5-triol
- English name
- 2-Deoxy-D-Glucose
- Molecular formula
- C6H12O5
- Molecular weight
- 164.16
Names & synonyms
2-Deoxy-alpha-D-arabino-hexopyranose13299-15-561R00HG0GBalpha-D-2-Deoxyglucopyranosealpha-D-2-Deoxymannopyranosealpha-D-Arabino-hexopyranose, 2-deoxy-RefChem:936082GlyTouCan:G58150MGG58150MG(2S,4R,5S,6R)-6-(hydroxymethyl)oxane-2,4,5-triolUNII-61R00HG0GB2-Deoxy-alpha-D-glucopyranose
Show more names
α-D-arabino-Hexopyranose, 2-deoxy-
2-desoxyglucoseZ612-deoxy-alpha-D-glucoseSCHEMBL4295810CHEMBL4303562CHEBI:125684(2S,4R,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,4,5-triolAKOS015856215
Database identifiers
- CAS
13299-15-5- PubChem CID
- 9062
- ChEMBL
CHEMBL4303562- ChEBI
CHEBI:125684- UNII
- 61R00HG0GB
- Nikkaji
- J81.590J
Properties
Computed structural properties
- XLogP
- -1.6
- Topological polar surface area
- 90.2 Ų
- Hydrogen bond donors
- 4
- Hydrogen bond acceptors
- 5
- Rotatable bonds
- 1
- Heavy atoms
- 11
- Formal charge
- 0
- Complexity
- 128
Physicochemical properties
- Melting point
- 175 °C · 175 °C
- Boiling point
- 411 · 411.0±45.0 °C(Predicted)
- Density
- 1.533 · 1.533±0.06 g/cm3(Predicted)
- pka
- 12 · 12+-.0.70(Predicted)
- FDA UNII
- 61 R00HG0GB · 61R00HG0GB
Chemistry & industry
Upstream & downstream products
Downstream products
Suppliers4 total
湖南韵邦生物科技股份有限公司0731-88532326 13319508186 · [email protected]
杭州璟皓生物科技有限公司（原河南辛迪加生物）17513242016 · [email protected]
Watson Biotechnology Co.,Ltd+86-18186686046 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
Additional notes
DefinitionChEBI: (2S,4R,5S,6R)-6-(hydroxymethyl)oxane-2,4,5-triol is a hexose.
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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