2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl bromide
α-D-Galactopyranosyl bromide, 2,3,4,6-tetrakis-O-(phenylmethyl)-
2,3,4,6-Tetra-O-benzyl-alpha-D-galactopyranosyl bromide,
(2R,3S,4S,5R,6R)-3,4,5-tris(benzyloxy)-2-[(benzyloxy)methyl]-6-bromooxane
2,3,4,6-Tetra-O-Benzyl-α-D-Galactopyranosyl Bromide, 
Catalog Number OM-5546
Product Name 2,3,4,6-Tetra-O-Benzyl-α-D-Galactopyranosyl Bromide,
CAS No. 53081-30-4
Aspect White powder
| CAS No. | 53081-30-4 |
| Molecular Formula | C34H35BrO5 |
| MW | 603.54 |
| Boiling Point | 667.1±55.0ºC(lit.) |
| Application | Pharmaceutical intermediate. |
| Synonyms | Tetrabenzyl-Α-D-galactopyranose bromide |
| SMILES | C1=CC=C(C=C1)COC[CH]2[CH]([CH]([CH]([CH](O2)Br)OCC3=CC=CC=C3)OCC4=CC=CC=C4)OCC5=CC=CC=C5 |
| InchiKey | WXYNLXPSTFTJJC-UHFFFAOYSA-N |
2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl bromide
α-D-Galactopyranosyl bromide, 2,3,4,6-tetrakis-O-(phenylmethyl)-
2,3,4,6-Tetra-O-benzyl-alpha-D-galactopyranosyl bromide,
(2R,3S,4S,5R,6R)-3,4,5-tris(benzyloxy)-2-[(benzyloxy)methyl]-6-bromooxane
·High purity (≥95%) ensuring consistent and reliable performance in various applications
·Protected galactose derivative with a bromide at the anomeric position, making it a versatile glycosyl donor
·Confirmed identity by MS/NMR, ensuring the accuracy of the product
·Biochemical Research: Used as a substrate or intermediate in various biochemical reactions.
·Organic Synthesis: Serves as a building block for the synthesis of complex organic compounds.
·Pharmaceutical Industry: Utilized in the development and production of pharmaceuticals.
·Oligosaccharide Synthesis: Acts as a glycosyl donor for the synthesis of α-galactosides
·2,3,4,6-Tetra-O-Acetyl-α-D-Galactopyranosyl Bromide: A similar compound with different protecting groups, used in related biochemical studies.
·Acetobromo-α-D-Galactose: A simpler derivative, often used in carbohydrate chemistry.
·2,3,4,6-Tetra-O-Benzoyl-α-D-Glucopyranosyl Bromide: A closely related compound with glucose instead of galactose, offering alternative applications in carbohydrate chemistry.
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