Methyl 4,4,4-Trichlorobutanoate

≥98%

Reagent Code: #83727
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CAS Number 19376-57-9

blur_circular Chemical Specifications

scatter_plot 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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days €57.47
inventory 1g
10-20 days €193.75
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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