Allyl 2,2,2-trichloroacetimidate
98%
- Product Code: 83164
CAS:
51479-73-3
| Molecular Weight: | 202.46 g./mol | Molecular Formula: | C₅H₆Cl₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00190710 | |
| Melting Point: | Boiling Point: | 145.5°C | |
| Density: | 1.36g/mL | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of the allyl group into various molecules. It is particularly effective in glycosylation reactions, where it facilitates the formation of glycosidic bonds, a critical step in the synthesis of complex carbohydrates and glycoconjugates. The compound is also employed in the preparation of allyl ethers and esters, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to act as a protective group for alcohols and amines further enhances its utility in multi-step synthetic processes. Additionally, it is used in the development of polymeric materials and coatings, where it contributes to the modification of surface properties and the enhancement of material performance.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Yellow Liquid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| REFRACTIVE INDEX N20D | 1.483-1.487 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $61.46 |
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| 5.000 | 10-20 days | $243.36 |
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| 25.000 | 10-20 days | $826.43 |
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Allyl 2,2,2-trichloroacetimidate
This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of the allyl group into various molecules. It is particularly effective in glycosylation reactions, where it facilitates the formation of glycosidic bonds, a critical step in the synthesis of complex carbohydrates and glycoconjugates. The compound is also employed in the preparation of allyl ethers and esters, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to act as a protective group for alcohols and amines further enhances its utility in multi-step synthetic processes. Additionally, it is used in the development of polymeric materials and coatings, where it contributes to the modification of surface properties and the enhancement of material performance.
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