4-Methylphenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside
≥98%
- Product Code: 103728
CAS:
28244-94-2
Molecular Weight: | 454.49074 g./mol | Molecular Formula: | C₂₁H₂₆O₉S |
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EC Number: | MDL Number: | MFCD13182351 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is primarily utilized in carbohydrate chemistry research, particularly in the synthesis of complex glycoconjugates. It serves as a key intermediate in the preparation of thioglycosides, which are essential for constructing oligosaccharides and glycoproteins. The acetyl groups protect the hydroxyl functionalities, allowing selective deprotection and further modification. It is also employed in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Additionally, it is used in the study of enzymatic glycosylation processes, aiding in understanding biochemical pathways.
Product Specification:
Test | Specification |
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Appearance | White To Off-White Solid |
Purity (%) | 97.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $37.20 |
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5.000 | 10-20 days | $163.22 |
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4-Methylphenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside
This chemical is primarily utilized in carbohydrate chemistry research, particularly in the synthesis of complex glycoconjugates. It serves as a key intermediate in the preparation of thioglycosides, which are essential for constructing oligosaccharides and glycoproteins. The acetyl groups protect the hydroxyl functionalities, allowing selective deprotection and further modification. It is also employed in the development of glycosidase inhibitors, which have potential therapeutic applications in treating diseases like diabetes and viral infections. Additionally, it is used in the study of enzymatic glycosylation processes, aiding in understanding biochemical pathways.
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