2,2,2-Trichloroethyl chloroformate
99%
- Product Code: 122797
Alias:
2,2,2-Trichloroethyl Chloroformate ;Trichloroethyl Chloroformate
CAS:
17341-93-4
| Molecular Weight: | 211.86 g./mol | Molecular Formula: | C₃H₂Cl₄O₂ |
|---|---|---|---|
| EC Number: | 241-363-7 | MDL Number: | MFCD00000810 |
| Melting Point: | 1°C | Boiling Point: | 171-172 °C(lit.) |
| Density: | 1.539 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
Used primarily in organic synthesis as a reagent for introducing the trichloroethyl protecting group. It is particularly valuable in peptide chemistry, where it helps protect amino acids during complex reactions, ensuring selective bond formation. The compound is also employed in the preparation of carbamates and carbonates, which are intermediates in the production of pharmaceuticals and agrochemicals. Its reactivity with alcohols and amines makes it a versatile tool for creating functionalized molecules. Additionally, it finds use in the synthesis of specialty chemicals and polymers, where controlled protection and deprotection steps are critical.
Product Specification:
| Test | Specification |
|---|---|
| Refractive Index N20/D | 1.469-1.471 |
| Specific Gravity (20/20 Degree Celsius) | 1.574-1.582 |
| Purity (T) | 98.5-101.5 |
| Appearance | Colorless Liquid |
| Infrared 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 |
|---|---|---|---|
| 5.000 | 10-20 days | £11.76 |
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| 25.000 | 10-20 days | £36.19 |
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| 100.000 | 10-20 days | £132.99 |
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| 500.000 | 10-20 days | £510.69 |
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2,2,2-Trichloroethyl chloroformate
Used primarily in organic synthesis as a reagent for introducing the trichloroethyl protecting group. It is particularly valuable in peptide chemistry, where it helps protect amino acids during complex reactions, ensuring selective bond formation. The compound is also employed in the preparation of carbamates and carbonates, which are intermediates in the production of pharmaceuticals and agrochemicals. Its reactivity with alcohols and amines makes it a versatile tool for creating functionalized molecules. Additionally, it finds use in the synthesis of specialty chemicals and polymers, where controlled protection and deprotection steps are critical.
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