Methyl 4,4,4-Trichlorobutanoate
≥98%
Reagent
Code: #83727
CAS Number
19376-57-9
blur_circular Chemical Specifications
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Molecular Information
Weight
205.47 g/mol
Formula
C₅H₇Cl₃O₂
thermostat
Physical Properties
Boiling Point
211.6ºC
inventory_2
Storage & Handling
Density
1.381g/cm3
Storage
room temperature, dry
description 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.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to light yellow liquid |
Purity | 97.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
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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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