1,3,4,6-Tetra-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-glucopyranose
98%
- Product Code: 242978
Alias:
(2S,3R,4R,5S,6R)-6-(acetoxymethyl)-3-(((2,2,2-trichloroethoxy)carbonyl)amino)tetrahydro-2H-pyran-2,4,5-triyltriacetate ester
CAS:
122210-05-3
| Molecular Weight: | 522.71 g./mol | Molecular Formula: | C₁₇H₂₂Cl₃NO₁₁ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21608553 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Dry |
Product Description:
Used as a key intermediate in the synthesis of complex carbohydrates and glycosaminoglycans, particularly in the preparation of heparin and heparan sulfate analogs. Its protected functional groups allow selective deprotection and coupling in oligosaccharide assembly. The trichloroethoxycarbonyl (Troc) group serves as a temporary protecting group for the amino function, which can be removed under mild reducing conditions without affecting other acetyl protections. This makes it valuable in stepwise solid-phase and solution-phase glycosylation strategies. Commonly employed in medicinal chemistry for developing anticoagulant and anti-inflammatory agents.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £25.07 |
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| 5.000 | 10-20 days | £250.75 |
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| 1.000 | 10-20 days | £66.11 |
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1,3,4,6-Tetra-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-glucopyranose
Used as a key intermediate in the synthesis of complex carbohydrates and glycosaminoglycans, particularly in the preparation of heparin and heparan sulfate analogs. Its protected functional groups allow selective deprotection and coupling in oligosaccharide assembly. The trichloroethoxycarbonyl (Troc) group serves as a temporary protecting group for the amino function, which can be removed under mild reducing conditions without affecting other acetyl protections. This makes it valuable in stepwise solid-phase and solution-phase glycosylation strategies. Commonly employed in medicinal chemistry for developing anticoagulant and anti-inflammatory agents.
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