5-Chloro-2-(trifluoromethyl)phenylacetonitrile

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Reagent Code: #166527
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CAS Number 261763-26-2

science Other reagents with same CAS 261763-26-2

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Weight 219.59 g/mol
Formula C₉H₅ClF₃N
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MDL Number MFCD01631357
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of agricultural chemicals, particularly in the production of certain herbicides and insecticides. Its structure allows for the introduction of trifluoromethyl and chloroaryl groups, which are common in agrochemical active ingredients due to their stability and bioactivity. It is also utilized in the development of pharmaceuticals where nitrile and halogenated aromatic moieties are needed for target molecule construction. The compound's reactivity makes it suitable for carbon-carbon bond formation in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,260.00
inventory 250mg
10-20 days ฿5,430.00
inventory 1g
10-20 days ฿14,160.00

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5-Chloro-2-(trifluoromethyl)phenylacetonitrile
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Used as an intermediate in the synthesis of agricultural chemicals, particularly in the production of certain herbicides and insecticides. Its structure allows for the introduction of trifluoromethyl and chloroaryl groups, which are common in agrochemical active ingredients due to their stability and bioactivity. It is also utilized in the development of pharmaceuticals where nitrile and halogenated aromatic moieties are needed for target molecule construction. The compound's reactivity makes it suitable

Used as an intermediate in the synthesis of agricultural chemicals, particularly in the production of certain herbicides and insecticides. Its structure allows for the introduction of trifluoromethyl and chloroaryl groups, which are common in agrochemical active ingredients due to their stability and bioactivity. It is also utilized in the development of pharmaceuticals where nitrile and halogenated aromatic moieties are needed for target molecule construction. The compound's reactivity makes it suitable for carbon-carbon bond formation in multi-step organic syntheses.

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