Structure via PubChem · Public domain (PubChem)
methyl D-glucoside
Sign in to saveAlso known as 1-O-methyl-D-glucopyranose, methylglucoside
Methylglucoside is a monosaccharide derived from glucose. It can be prepared in the laboratory by the acid-catalyzed reaction of glucose with methanol.
In the Vinony graph
Within Vinony's link graph, methyl D-glucoside is referenced by 14 other articles, and connects out to carbohydrate, mass density and glucose.
Vinony files it under Chemical articles with multiple CAS registry numbers, Chemical articles with multiple compound IDs and ECHA InfoCard ID from Wikidata.
Its subject is documented across 5 Wikipedia language editions.
Chemical data
- Formula
- C7H14O6
- Molecular weight
- 194.18 g/mol
- IUPAC name
- (2R,3S,4S,5R)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol
- SMILES
- COC1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
- InChIKey
- HOVAGTYPODGVJG-WLDMJGECSA-N
- XLogP
- -2.2
- Polar surface area
- 99.4 Ų
- H-bond donors
- 4
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 194.079
Show 5 more facts
- Commons category
- Methylglucoside
- chemical formula
- C₇H₁₄O₆
- isomeric SMILES
- COC1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
- canonical SMILES
- COC1C(C(C(C(O1)CO)O)O)O
- found in taxon
- Hordeum vulgare
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Methylglucoside is a monosaccharide derived from glucose. It can be prepared in the laboratory by the acid-catalyzed reaction of glucose with methanol.
It is used as a chemical intermediate in the production of a variety of products including emollients, emulsifiers, humectants, moisturizers, thickening agents, plasticizers, surfactants, varnishes, and resins. The formation of methyl glycoside indicates that the structure of glucose is not open chain.
Excerpted from Wikipedia’s “methyl D-glucoside” article, available under the CC BY-SA 4.0 licence.