Basic information
- CAS
18403-12-8- Standard SMILES
OC1COC(OCc2ccccc2)C(O)C1O- InChIKey
XUGMDBJXWCFLRQ-WISYIIOYSA-N- Molecular formula
- C12H16O5
- Average molar mass
- 240.25 g/mol
- Monoisotopic mass
- 240.09977361
Names & identifiers
- Preferred name
- 2-Phenylmethoxyoxane-3,4,5-triol
- IUPAC
- 2-phenylmethoxyoxane-3,4,5-triol
- English name
- BENZYL-BETA-L-ARABINOPYRANOSIDE
- Molecular formula
- C12H16O5
- Molecular weight
- 240.25
Names & synonyms
NSC25617473-38-3Benzyl -D-arabinopyranosideBenzyl beta-D-ribopyranosideBenzyl beta-L-ribopyranosidebenzyl beta-l-arabinopyranosideMLS000736490benzyl pentopyranoside2-phenylmethoxyoxane-3,4,5-triol70797-93-261134-26-7Oprea1_820628
Show more names
Benzylb-L-arabinopyranosideBenzyl β-D-Arabinopyranoside1-O-BENZYL-BETA-D-ARABINOSIDEPhenylmethyl β-D-arabinopyranosideβ-D-Arabinopyranoside, phenylmethyl2-BENZYLOXY-TETRAHYDRO-PYRAN-3,4,5-TRIOLBenzyl beta-D-arabinopyranoside, Min. 98%Benzyl β-D-Arabinopyranoside, CAS 5329-50-0
CHEMBL1710955SCHEMBL14356311HMS2819E07MFCD06200793NSC170150NSC231837NSC400277NSC-170150
Database identifiers
- CAS
18403-12-8、5329-50-0、70797-93-2、7473-38-3- PubChem CID
- 220191
- ChEMBL
CHEMBL1710955
Properties
Computed structural properties
- XLogP
- -0.5
- Topological polar surface area
- 79.2 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 5
- Rotatable bonds
- 3
- Heavy atoms
- 17
- Formal charge
- 0
- Complexity
- 229
Physicochemical properties
- Melting point
- 169 · 169-173°C
- Boiling point
- 418.507 · 418.507±45.00 °C(Press: 760.00 Torr)(predicted)
- Density
- 1.354 · 1.354±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
- storage temp.
- Refrigerator
- solubility
- DMSO, Methanol, Water
- form
- Solid
- pka
- 13.045 · 13.045±0.70(predicted)
- color
- White to Off-White
Chemistry & industry
Applications
UsesPhenylmethyl β-D-arabinopyranoside 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].
Upstream & downstream products
Downstream products
Suppliers5 total
陕西缔都医药有限责任公司029-81124775 17791530730 · [email protected]
武汉开诺医药科技有限公司18040571231/1402788087
北京秦岭医药科技有限公司010-61241352 18901327973 · [email protected]
成都金麦瑞生物科技有限公司028-83133020 18280298385 · [email protected]
HANGZHOU LEAP CHEM CO., LTD.+86-571-87711850 +86-15355479329 · [email protected]
Related reactions
0 records
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Compound notes
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