| Weight | 162.141 g/mol |
|---|---|
| Formula | C6H10O5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,6-Anhydro-beta-D-glucopyranose (498-07-7)
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- Sigma-Aldrich - 1,6-Anhydro-beta-D-glucopyranose81.60 - 382.20 USD
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- TCI - 1,6-Anhydro-beta-D-glucopyranose65.00 - 193.00 USD
- Thermal degradation of 1,6-anhydro-.beta.-D-glucopyranose (Journal of Organic Chemistry, 1972)
- Steric control in the polymerization of 1,6-anhydro-.beta.-D-glucopyranose derivatives (Journal of the American Chemical Society, 1969)
- Ring-opening polymerization of 1,4-anhydro-2,3,6-tri-0-benzyl-.alpha.-D-glucopyranose and 1,4-anhydro-2,3,6-tri-0-benzyl-.beta.-D-galactopyranose (Macromolecules, 1985)
- Studies in the ganglioside series. IV. Preparation of 2,3-di-O-acetyl-1,6-anhydro-beta-D-glucopyranose and its utilization in the synthesis of oligosaccharides. (Journal of Organic Chemistry, 1970)
- Facile Preparation of 1,6-Anhydro-2-azido-3-O-benzyl-2-deoxy-.BETA.-D-glucopyranose and Its 4-O-Substituted Derivatives. (Bulletin of the Chemical Society of Japan, 1994)
- Polymerization of 1,3-anhydro-2,4,6-tri-O-benzyl-.beta.-D-glucopyranose, a substituted 2,6-dioxabicyclo[3.1.1]heptane (Macromolecules, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C2C(C(C(C(O1)O2)O)O)O
-
InChIKeyTWNIBLMWSKIRAT-UHFFFAOYSA-N
- Pubchem - 1,6-Anhydro-beta-D-glucopyranose
- Wikipedia - levoglucosan
Levoglucosan (C6H10O5) is an organic compound with a six-carbon ring structure formed from the pyrolysis of carbohydrates, such as starch and cellulose. As a result, levoglucosan is often used as a chemical tracer for biomass burning in atmospheric chemistry studies, particularly with respect to airborne particulate matter. Along with other tracers such as potassium, oxalate, and gaseous acetonitrile, levoglucosan has been shown to be highly correlated with regional fires.
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1,6-Anhydro-beta-D-glucopyranose
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