M8031
Methyl 2,3,4,6-tetra-O-acetyl-β-D-thiogalactopyranoside
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About This Item
form
solid
storage temp.
−20°C
SMILES string
CS[C@@H]1O[C@H](COC(C)=O)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
InChI
1S/C15H22O9S/c1-7(16)20-6-11-12(21-8(2)17)13(22-9(3)18)14(23-10(4)19)15(24-11)25-5/h11-15H,6H2,1-5H3/t11-,12+,13+,14-,15+/m1/s1
InChI key
XWFUCHLBRWBKGN-FQKPHLNHSA-N
Application
Methyl 2,3,4,6-tetra-O-acetyl-β-D-thiogalactopyranoside has been used in a study to assess applications of ionic liquids in carbohydrate chemistry. It has also been used to study thioglycosylation in ionic liquids.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Beilstein journal of organic chemistry, 2, 12-12 (2006-06-29)
A novel, green chemistry, glycosylation strategy was developed based upon the use of ionic liquids. Research studies demonstrated that thiomethyl glycosides could readily be activated with methyl trifluoromethane sulfonate, using 1-butyl-3-methylimidazolium tetrafluoroborate as a solvent. This green chemistry glycosylation strategy
Biomacromolecules, 8(9), 2629-2647 (2007-08-19)
Ionic liquids (ILs) are composed only of ions. Of special interest to this review are those where at least one ion (the cation) is organic and whose melting points are below or not far above room temperature. ILs are designated
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