2,3,4,6-Tetra-O-benzyl-D-galactopyranose
≥98%
- Product Code: 103647
CAS:
6386-24-9
| Molecular Weight: | 540.66 g./mol | Molecular Formula: | C₃₄H₃₆O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00132927 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates, it plays a crucial role in the development of glycobiology research. It is particularly valuable in the preparation of glycosyl donors for oligosaccharide synthesis, enabling the study of carbohydrate-protein interactions. This compound is also employed in the pharmaceutical industry for the production of glycosylated drugs and vaccines, enhancing their efficacy and stability. Additionally, it aids in the creation of glycomimetics, which are used to design therapeutic agents targeting diseases like cancer and infections. Its benzyl protecting groups facilitate selective reactions, making it a versatile tool in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (%) | 97.5-100 |
| Specific Rotation [A]20/D(C=1,CHCL3) | 9.0-13.0 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿1,810.00 |
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| 1.000 | 10-20 days | ฿5,520.00 |
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2,3,4,6-Tetra-O-benzyl-D-galactopyranose
Used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates, it plays a crucial role in the development of glycobiology research. It is particularly valuable in the preparation of glycosyl donors for oligosaccharide synthesis, enabling the study of carbohydrate-protein interactions. This compound is also employed in the pharmaceutical industry for the production of glycosylated drugs and vaccines, enhancing their efficacy and stability. Additionally, it aids in the creation of glycomimetics, which are used to design therapeutic agents targeting diseases like cancer and infections. Its benzyl protecting groups facilitate selective reactions, making it a versatile tool in organic synthesis.
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