2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide

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2
(4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate)

2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide

Original price was: $995.00.Current price is: $495.00.

Catalog Number: B2027270 (1 g)
2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide is a versatile carbohydrate intermediate and glycosyl donor widely used in stereoselective glycosylation reactions. It plays a key role in the chemical synthesis of complex oligosaccharides, glycoconjugates, and functionalized galactosides. Supplied as a high-purity crystalline solid, this reagent is essential for carbohydrate chemistry and biochemical research applications. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide
Catalog number: B2027270
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 411.21
Supplied as: Powder
Storage: NA
Keywords: Acetobromo-α-D-galactose, Acetobromogalactose, Acetobromo-a-D-galactose

References:
1. Koenigs W, Knorr E. Über einige Derivate der Traubenzucker und Galactose. Berichte der deutschen chemischen Gesellschaft. 1901;34(1):957-981.
2. Lemieux RU, Hendriks KB, Stick RV, Kohner K. Halide ion catalyzed glycosylation. Journal of the American Chemical Society. 1975;97(14):4056-4062.
3. Kartha KP, Jennings HJ. A convenient synthesis of 2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl bromide. Journal of Carbohydrate Chemistry. 1990;9(5):777-781.
4. Haynes LJ, Todd AR. Codeimane and related compounds. Part I. Synthesis of galactopyranosyl derivatives. Journal of the Chemical Society. 1950;1950:303-308.
5. Toshima K, Tatsuta K. Recent progress in O-glycosylation methods. Chemical Reviews. 1993;93(4):1503-1531.
6. Barresi F, Hindsgaul O. Synthesis of beta-D-galactopyranosides from acylated galactopyranosyl bromides. Canadian Journal of Chemistry. 1994;72(6):1447-1454.
7. Cron S, Pavia AA. Glycosylation of amino acids using 2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl bromide. Tetrahedron Letters. 1979;20(23):2121-2124.
8. Garegg PJ. Thioglycosides as glycosyl donors in oligosaccharide synthesis. Advances in Carbohydrate Chemistry and Biochemistry. 1997;52:179-205.
9. Flowerdew AW, Thomas EL. Synthesis of alpha-D-galactopyranosides using galactopyranosyl halides. Carbohydrate Research. 1989;190(2):165-172.
10. Paulsen H. Advances in selective chemical syntheses of complex oligosaccharides. Angewandte Chemie International Edition. 1982;21(3):155-173.
2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide

Products Related to 2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide can be found at Carbohydrates

Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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