Methyl 4,4,4-Trichlorobutanoate
≥98%
- Product Code: 83727
CAS:
19376-57-9
| Molecular Weight: | 205.47 g./mol | Molecular Formula: | C₅H₇Cl₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 211.6ºC | |
| Density: | 1.381g/cm3 | Storage Condition: | room temperature, dry |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various agrochemicals and pharmaceuticals. Its trichlorinated structure makes it valuable for introducing trichloromethyl groups into more complex molecules, which can enhance biological activity or stability. In agrochemicals, it is often utilized to develop herbicides and pesticides, leveraging its reactivity to create compounds that target specific pests or weeds. In pharmaceuticals, it aids in the synthesis of active ingredients, particularly those requiring trichloromethyl functionalities for therapeutic effects. Additionally, it finds application in research settings for studying reaction mechanisms involving halogenated esters.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to light yellow Liquid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $85.73 |
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| 1.000 | 10-20 days | $289.05 |
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Methyl 4,4,4-Trichlorobutanoate
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various agrochemicals and pharmaceuticals. Its trichlorinated structure makes it valuable for introducing trichloromethyl groups into more complex molecules, which can enhance biological activity or stability. In agrochemicals, it is often utilized to develop herbicides and pesticides, leveraging its reactivity to create compounds that target specific pests or weeds. In pharmaceuticals, it aids in the synthesis of active ingredients, particularly those requiring trichloromethyl functionalities for therapeutic effects. Additionally, it finds application in research settings for studying reaction mechanisms involving halogenated esters.
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