3-chloro-2-[3-(trifluoromethyl)-1H-pyrazol-1-yl]pyridine

95%

Reagent Code: #196399
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CAS Number 438450-38-5

science Other reagents with same CAS 438450-38-5

blur_circular Chemical Specifications

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Weight 247.61 g/mol
Formula C₉H₅ClF₃N₃
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fungicides and insecticides. Its structure enables effective binding to biological targets, enhancing the activity of active ingredients in crop protection products. It is also utilized in the preparation of novel heterocyclic compounds with potential medicinal properties, including anti-inflammatory and antimicrobial agents. The compound’s stability and reactivity make it suitable for use in cross-coupling reactions during drug discovery processes.

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inventory 1g
10-20 days ฿11,400.00

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3-chloro-2-[3-(trifluoromethyl)-1H-pyrazol-1-yl]pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fungicides and insecticides. Its structure enables effective binding to biological targets, enhancing the activity of active ingredients in crop protection products. It is also utilized in the preparation of novel heterocyclic compounds with potential medicinal properties, including anti-inflammatory and antimicrobial agents. The compound’s stability and reactivity make it suitable for use

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fungicides and insecticides. Its structure enables effective binding to biological targets, enhancing the activity of active ingredients in crop protection products. It is also utilized in the preparation of novel heterocyclic compounds with potential medicinal properties, including anti-inflammatory and antimicrobial agents. The compound’s stability and reactivity make it suitable for use in cross-coupling reactions during drug discovery processes.

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