2-Chloro-5-(trifluoromethyl)benzyl alcohol

98%

Reagent Code: #158970
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CAS Number 64372-62-9

science Other reagents with same CAS 64372-62-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.58 g/mol
Formula C₈H₆ClF₃O
badge Registry Numbers
MDL Number MFCD01631469
thermostat Physical Properties
Melting Point 57-60°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agricultural chemicals, particularly in the production of certain herbicides and insecticides. Its structure allows for effective modification to create active ingredients that target specific pests or weeds. Commonly utilized in the development of pyrethroid-like compounds due to the benzyl alcohol moiety, which enhances bioavailability and binding efficiency. Also serves as a building block in medicinal chemistry for creating fluorinated analogs with improved metabolic stability. Frequently employed in research settings for designing new agrochemical candidates with enhanced environmental persistence and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿600.00
25g
10-20 days ฿2,950.00
2-Chloro-5-(trifluoromethyl)benzyl alcohol
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Used as a key intermediate in the synthesis of agricultural chemicals, particularly in the production of certain herbicides and insecticides. Its structure allows for effective modification to create active ingredients that target specific pests or weeds. Commonly utilized in the development of pyrethroid-like compounds due to the benzyl alcohol moiety, which enhances bioavailability and binding efficiency. Also serves as a building block in medicinal chemistry for creating fluorinated analogs with impro

Used as a key intermediate in the synthesis of agricultural chemicals, particularly in the production of certain herbicides and insecticides. Its structure allows for effective modification to create active ingredients that target specific pests or weeds. Commonly utilized in the development of pyrethroid-like compounds due to the benzyl alcohol moiety, which enhances bioavailability and binding efficiency. Also serves as a building block in medicinal chemistry for creating fluorinated analogs with improved metabolic stability. Frequently employed in research settings for designing new agrochemical candidates with enhanced environmental persistence and selectivity.

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