4-Methoxybenzyl 2,2,2-Trichloroacetimidate
≥96%(GC)
- Product Code: 83165
CAS:
89238-99-3
| Molecular Weight: | 282.55 g./mol | Molecular Formula: | C₁₀H₁₀Cl₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00134547 | |
| Melting Point: | Boiling Point: | 137°C|0.7mmHg(lit.) | |
| Density: | 1.36 | Storage Condition: | -20°C, inert gas |
Product Description:
Used as a key reagent in organic synthesis for the protection of hydroxyl groups, particularly in carbohydrate chemistry. It facilitates the formation of glycosidic bonds, enabling the synthesis of complex oligosaccharides and glycoconjugates. Its role in protecting sensitive functional groups ensures high selectivity and yield in multi-step reactions. Additionally, it is employed in the preparation of glycosyl donors, which are essential intermediates in the production of natural products and pharmaceuticals. Its stability and reactivity make it a valuable tool in the development of biologically active compounds and drug discovery.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Light yellow to Light orange clear liquid |
| PURITY | 95.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,770.00 |
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| 5.000 | 10-20 days | ฿5,910.00 |
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| 25.000 | 10-20 days | ฿24,290.00 |
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4-Methoxybenzyl 2,2,2-Trichloroacetimidate
Used as a key reagent in organic synthesis for the protection of hydroxyl groups, particularly in carbohydrate chemistry. It facilitates the formation of glycosidic bonds, enabling the synthesis of complex oligosaccharides and glycoconjugates. Its role in protecting sensitive functional groups ensures high selectivity and yield in multi-step reactions. Additionally, it is employed in the preparation of glycosyl donors, which are essential intermediates in the production of natural products and pharmaceuticals. Its stability and reactivity make it a valuable tool in the development of biologically active compounds and drug discovery.
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