Produktinformation
- (1R,2S,3S,4R,5R)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol
- 1,6-Anhydro-<span class="text-smallcaps">D</span>-glucopyranoside
- 1,6-Anhydro-<span class="text-smallcaps">D</span>-glucose
- 1,6-Anhydro-Beta-D-Glucopyranose
- 1,6-Anhydro-D-glucopyranoside
- 1,6-Anhydro-D-glucose
- 1,6-Anhydro-β-<span class="text-smallcaps">D</span>-glucopyranose
- 1,6-Anhydro-β-<span class="text-smallcaps">D</span>-glucose
- 1,6-Anhydroglucose
- 1,6-anhidro-β-D-glucosa
- Mehr Synonyme anzeigen
- 6,8-Dioxabicyclo[3.2.1]octane, β-<span class="text-smallcaps">D</span>-glucopyranose deriv.
- <span class="text-smallcaps">D</span>-Glucose, 1,6-anhydro-
- D-Glucose, 1,6-anhydro-
- GLUCOPYRANOSE (,beta.-D), 1,6-ANHYDRO-
- Leucoglucosan
- Levoglucosan
- Nsc 46243
- β-<span class="text-smallcaps">D</span>-Glucopyranose, 1,6-anhydro-
- β-D-Glucopyranose, 1,6-anhydro-
Stability Hygroscopic
Applications 1,6-Anhydrohexopyranoses have proven to be valuable synthons for the preparation of biologically important and structurally diverse products (e.g. rifamycin S, indanomycin, thromboxane B2, (+)-biotin, tetrodotoxin, quinone, and macrolide antibiotics) as well as for modified sugars.The chemical/physical/toxicological properties have not been thoroughly investigated. Since it is known to be a minor component of certain food materials it may be regarded as of relatively low toxicity.
References Fraser-Reid, B., et al. J. Am. Chem. Soc. 106, 731 (1984); Edwards, M.P., et al. J. Org. Chem. 49, 3503 (1984); Kelly, A.G., and Roberts, J.S. J. Chem. Soc., Chem. Commun. 228, (1980); Ogawa, T., et al. Carbohydr. Res. 57, C31 (1977); Isobe, M., et al. Tetrahedron Lett. 28, 6485 (1987); Fresnos, J.N. and Swenton, J.S. , J. Chem. Soc., Chem. Commun. 658, (1985); Kochetkov, N.K. et al., Tetrahedron Lett. 22, 4315, 4319 (1981); Georges, M. et al., Carbohydr. Res. 130, 115 (1984); Paulsen, et al., Chem. Ber. 114, 322 (1981).
Chemische Eigenschaften
Technische Anfrage zu: TR-A648100 1,6-Anhydro-β-D-glucopyranose
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