Molecular structure of 1,3,4,6-Tetra-O-acetyl-α-D-galactopyranose, CAS Number: 19186-40-4
1,3,4,6-Tetra-O-acetyl-α-D-galactopyranose (CAS 19186-40-4)
Application:
1,3,4,6-Tetra-O-acetyl-α-D-galactopyranose is a derivative of galactopyranose
CAS Number:
19186-40-4
Molecular Weight:
348.30
Molecular Formula:
C14H20O10
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
1,3,4,6-Tetra-O-acetyl-α-D-galactopyranose is a chemical compound that belongs to the family of carbohydrates. It is a derivative of α-D-galactopyranose, where the hydroxyl groups at positions 1, 3, 4, and 6 are acetylated. This compound is used as a building block or precursor in organic synthesis and carbohydrate chemistry.
1,3,4,6-Tetra-O-acetyl-α-D-galactopyranose (CAS 19186-40-4) References
- Synthesis of a Conjugation-Ready, Phosphorylated, Tetrasaccharide Fragment of the O-PS of Vibrio cholerae O139. | Soliman, SE. and Kováč, P. 2015. J Org Chem. 80: 11227-32. PMID: 26528773
- Stereoselective trimethylsilylation of α- and β-galactopyranoses. | Asami, Y., et al. 2019. Carbohydr Res. 474: 51-56. PMID: 30731331
- Synthesis of carbohydrate building blocks via regioselective uniform protection/deprotection strategies. | Wang, T. and Demchenko, AV. 2019. Org Biomol Chem. 17: 4934-4950. PMID: 31044205
- Synthesis of the hexasaccharide from Trypanosoma cruzi mucins with the Galp(1 → 2)Galf unit constructed with a superarmed thiogalactopyranosyl donor. | Kashiwagi, GA., et al. 2019. Carbohydr Res. 482: 107734. PMID: 31271957
- Di- and tri-saccharide glycosyl donors for the synthesis of fragments of the O-specific antigen of Shigella dysenteriae type 1. | Kovác, P. 1993. Carbohydr Res. 245: 219-31. PMID: 7690306
- Treatment of 1, 3, 4, 6-tetra-O-acetyl-α-d-galactopyranose and-α-d-glucopyranose with methyl sulphoxide-acetic anhydride; formation of kojic acid diacetate. | Chittenden, G. J. F. 1969. Carbohydrate Research. 11.3: 424-427.
- Benzyl trifluoromethanesulfonate. Preparation of tri-O-acetyl-2-O-benzyl-α-d-galactopyranosyl bromide from 1,3,4,6-tetra-O-acetyl-α-d-galactopyranose. | Lemieux R.U., Kondo T. 1974. Carbohydr. Res. 35: C4-C6.
- Stereoselective Ring-Opening of Acetylated Pyranose-1, 2-(ethyl orthoacetates). | SAITO, Setsuo, et al. 1993. Chemical and pharmaceutical bulletin. 41.1: 90-96.
- A new glycosylation strategy for the synthesis of mannopyranosides. | Singh, Gurdial and Hariprasad Vankayalapati. 2000. Tetrahedron: Asymmetry. 11.1: 125-138.
- Neighboring group participation in glycosylation reactions by 2, 6-disubstituted 2-O-benzoyl groups: A mechanistic investigation. | Williams, Rohan J., et al. 2010. Journal of Carbohydrate Chemistry. 29.5: 236-263.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,3,4,6-Tetra-O-acetyl-α-D-galactopyranose, 100 mg | sc-220550 | 100 mg | $329.00 |