| Identification | Back Directory | [Name]
BENZYL 2,3-O-ISOPROPYLIDENE-6-TRITYL-ALPHA-D-MANNOFURANOSE | [CAS]
91364-11-3 | [Synonyms]
Benzyl2,3-O-isopropylidene-6-trityl-a-D-mannofuranose
Benzyl 2,3-O-Isopropylidene-6-O-trityl-α-D-mannofuranose
BENZYL 2,3-O-ISOPROPYLIDENE-6-TRITYL-ALPHA-D-MANNOFURANOSE
PhenylMethyl 2,3-O-(1-Methylethylidene)-6-O-(triphenylMethyl)-α-D-Mannofuranoside
α-D-Mannofuranoside, phenylmethyl 2,3-O-(1-methylethylidene)-6-O-(triphenylmethyl)- | [Molecular Formula]
C35H36O6 | [MDL Number]
MFCD09750721 | [MOL File]
91364-11-3.mol | [Molecular Weight]
552.66 |
| Chemical Properties | Back Directory | [Boiling point ]
659.645±55.00 °C(Press: 760.00 Torr)(predicted) | [density ]
1.255±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | [solubility ]
soluble in Chloroform, Dichloromethane | [form ]
Solid | [pka]
13.231±0.20(predicted) | [color ]
White |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Benzyl 2,3-O-Isopropylidene-6-O-trityl-α-D-mannofuranose 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 |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
|