3-(Trifluoromethyl)-1H-pyrazole-4-carbonitrile

≥95%

Reagent Code: #117495
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CAS Number 318951-60-9

science Other reagents with same CAS 318951-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.08 g/mol
Formula C₅H₂F₃N₃
badge Registry Numbers
MDL Number MFCD00231871
thermostat Physical Properties
Boiling Point 302.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its trifluoromethyl and cyano groups enhance the metabolic stability, lipophilicity, and electron-withdrawing properties of the resulting molecules, making it valuable in the development of drugs targeting central nervous system disorders, inflammation, and cancer. Additionally, it serves as a building block in agrochemical research for creating pesticides and herbicides with improved efficacy and selectivity. The compound’s unique structure also finds utility in material science, particularly in the design of advanced polymers and coatings with enhanced chemical resistance and durability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,926.00
inventory 1g
10-20 days ฿11,592.00
inventory 250mg
10-20 days ฿4,617.00

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3-(Trifluoromethyl)-1H-pyrazole-4-carbonitrile
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This chemical is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its trifluoromethyl and cyano groups enhance the metabolic stability, lipophilicity, and electron-withdrawing properties of the resulting molecules, making it valuable in the development of drugs targeting central nervous system disorders, inflammation, and cancer. Additionally, it serves as a building block in agrochemical research for creating pesticides and herbicides with

This chemical is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its trifluoromethyl and cyano groups enhance the metabolic stability, lipophilicity, and electron-withdrawing properties of the resulting molecules, making it valuable in the development of drugs targeting central nervous system disorders, inflammation, and cancer. Additionally, it serves as a building block in agrochemical research for creating pesticides and herbicides with improved efficacy and selectivity. The compound’s unique structure also finds utility in material science, particularly in the design of advanced polymers and coatings with enhanced chemical resistance and durability.

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