tert-Butyl 2,2,2-trichloroacetimidate
97%
- Product Code: 122377
Alias:
tert-Butyl 2,2,2-trichloroimidoacetate
tert-butyl trichloroacetimidate
CAS:
98946-18-0
| Molecular Weight: | 218.51 g./mol | Molecular Formula: | C₆H₁₀Cl₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00077410 | |
| Melting Point: | 21 °C(lit.) | Boiling Point: | 65 °C11 mm Hg(lit.) |
| Density: | 1.222 | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily used in organic synthesis as a reagent for the introduction of the tert-butoxycarbonyl (Boc) protecting group. It is particularly valuable in peptide synthesis, where it helps protect amine groups during the formation of peptide bonds, preventing unwanted side reactions. Additionally, it is employed in the preparation of glycosyl donors for carbohydrate chemistry, facilitating the synthesis of complex sugars. Its reactivity and stability make it a useful tool in the development of pharmaceuticals and fine chemicals.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 97-100 |
| Purity (Titration By Agno3 After O2 Combustion) | 96.5-103.5 |
| Purity (Titration By Agno3 After O2 Combustion) | 96.5-103.5 |
| Refractive Index N20/D | 1.454-1.458 |
| Specific Gravity (20/20 Degree Celsius) | 1.218-1.224 |
| Appearance | Colorless To Pale Yellow Liquid Or Solid |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
| Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft3,447.71 |
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| 5.000 | 10-20 days | Ft5,494.80 |
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| 25.000 | 10-20 days | Ft20,794.03 |
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| 100.000 | 10-20 days | Ft80,590.33 |
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tert-Butyl 2,2,2-trichloroacetimidate
This chemical is primarily used in organic synthesis as a reagent for the introduction of the tert-butoxycarbonyl (Boc) protecting group. It is particularly valuable in peptide synthesis, where it helps protect amine groups during the formation of peptide bonds, preventing unwanted side reactions. Additionally, it is employed in the preparation of glycosyl donors for carbohydrate chemistry, facilitating the synthesis of complex sugars. Its reactivity and stability make it a useful tool in the development of pharmaceuticals and fine chemicals.
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