Molecular structure of 1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose, CAS Number: 10548-46-6
1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose (CAS 10548-46-6)
Application:
1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose is a useful synthon for the preparation of a variety of compounds
CAS Number:
10548-46-6
Molecular Weight:
432.51
Molecular Formula:
C27H28O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
1,6-Anhydrohexopyranoses have proven to be valuable synthons for the preparation of biologically important and structurally diverse products such as rifamycin S, indanomycin, thromboxane B2, (+)-biotin, tetrodotoxin, quinone, and macrolide antibiotics.
1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose (CAS 10548-46-6) References
- Ring-opening polymerization of new 3-O-branched 1, 6-anhydro glucopyranose di- and trisaccharide monomers. | Bai, C., et al. 2017. Carbohydr Res. 446-447: 52-60. PMID: 28527419
- A biomimetic synthesis of (+)-biotin from D-glucose. | Ogawa, T., et al. 1977. Carbohydr Res. 57: C31-5. PMID: 902272
- Synthesis of sulfonated amino-polysaccharides having anti-HIV and blood anticoagulant activities. | Hattori, K., et al. 1998. Carbohydr Res. 312: 1-8. PMID: 9836449
- Synthesis of 2, 3, 4‐tri‐O‐benzyl‐[1→ 6]‐α‐d‐glucopyranan and [1→ 6]‐α‐d‐glucopyranan with high molecular weight by polymerization of 1, 6‐anhydro‐2, 3, 4‐tri‐O‐benzyl‐β‐d‐glucopyranose | Uryu, T., Tachikawa, H., Ohaku, K. I., Terui, K., & Matsuzaki, K. 1977. Die Makromolekulare Chemie: Macromolecular Chemistry and Physics. 178(7): 1929-1940.
- 31P and 19F NMR spectroscopic studies on ring‐opening polymerization of 1, 6‐anhydro‐2, 3, 4‐tri‐O‐benzyl‐β‐d‐glucopyranose by PF5 catalyst | Uryu, T., Ito, K., Kobayashi, K. I., & Matsuzaki, K. 1979. Die Makromolekulare Chemie: Macromolecular Chemistry and Physics. 180(6): 1509-1519.
- Graft copolymerization of anhydro sugar derivatives from macromolecular halides | Uryu, T., Hagino, A., Terui, K., & Matsuzaki, K. 1981. Journal of Polymer Science: Polymer Chemistry Edition. 19(9): 2313-2329.
- 1, 6-Anhydro-β-D-glucopyranose derivatives as glycosyl donors for thioglycosidation reactions | Wang, L. X., Sakairi, N., & Kuzuhara, H. 1990. Journal of the Chemical Society, Perkin Transactions 1. 6: 1677-1682.
- Cationic ring‐opening polymerization of new 1, 6‐anhydro‐β‐lactose derivatives | Yoshida, T., Yasuda, Y., Hattori, K., & Uryu, T. 1995. Macromolecular rapid communications. 16(12): 881-890.
- Synthesis of a (1→ 6)-β-Linked N-Acetyl-d-glucosamine Oligosaccharide1 | Kanno, K. I., Kobayashi, Y., Nishimura, S. I., Kuzuhara, H., & Hatanaka, K. 1995. Carbohydrate Chemistry. 14(4-5): 481-490.
- Ring-Opening Polymerization of a Benzylated 1, 6-Anhydro-β-d-talopyranose and Synthesis of a New Polysaccharide,(1→ 6)-α-d-Talopyranan | Hattori, K., & Yoshida, T. 2009. Macromolecules. 42(16): 6044-6049.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,6-Anhydro-2,3,4-tri-O-benzyl-β-D-glucopyranose, 1 g | sc-220566 | 1 g | $300.00 |