4-(Difluoromethyl)-N-hydroxybenzimidoyl chloride

95%

Reagent Code: #178692
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CAS Number 596095-16-8

science Other reagents with same CAS 596095-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.59 g/mol
Formula C₈H₆ClF₂NO
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of fungicides and herbicides. Its structure allows for the introduction of difluoromethyl groups, which can enhance metabolic stability and bioavailability in active ingredients. Commonly employed in condensation reactions to form oxime derivatives and heterocyclic compounds with biological activity. Also utilized in research settings for designing enzyme inhibitors due to the reactivity of the hydroxylamine and imidoyl chloride functional groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿31,060.00
inventory 250mg
10-20 days ฿51,530.00

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4-(Difluoromethyl)-N-hydroxybenzimidoyl chloride
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of fungicides and herbicides. Its structure allows for the introduction of difluoromethyl groups, which can enhance metabolic stability and bioavailability in active ingredients. Commonly employed in condensation reactions to form oxime derivatives and heterocyclic compounds with biological activity. Also utilized in research settings for designing enzyme inhibitors due to the reactivity of t

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of fungicides and herbicides. Its structure allows for the introduction of difluoromethyl groups, which can enhance metabolic stability and bioavailability in active ingredients. Commonly employed in condensation reactions to form oxime derivatives and heterocyclic compounds with biological activity. Also utilized in research settings for designing enzyme inhibitors due to the reactivity of the hydroxylamine and imidoyl chloride functional groups.

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