3-Chloro-5-(trifluoromethyl)-1H-1,2,4-triazole

95%

Reagent Code: #164584
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CAS Number 1199215-88-7

science Other reagents with same CAS 1199215-88-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.51 g/mol
Formula C₃HClF₃N₃
badge Registry Numbers
MDL Number MFCD13248683
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of triazole-based systemic fungicides that protect crops from fungal diseases. Its structure enables effective disruption of ergosterol biosynthesis in fungi, making it valuable in developing plant protection agents. Also utilized in the preparation of pharmaceutical compounds where triazole rings contribute to biological activity, especially in antimicrobial and anti-inflammatory agents. Its trifluoromethyl and chloro functional groups enhance metabolic stability and lipophilicity, improving efficacy in agrochemical and medicinal applications.

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Test Parameter Specification
Appearance solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,880.00
3-Chloro-5-(trifluoromethyl)-1H-1,2,4-triazole
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Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of triazole-based systemic fungicides that protect crops from fungal diseases. Its structure enables effective disruption of ergosterol biosynthesis in fungi, making it valuable in developing plant protection agents. Also utilized in the preparation of pharmaceutical compounds where triazole rings contribute to biological activity, especially in antimicrobial and anti-inflammatory agents. Its trifluorom

Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the production of triazole-based systemic fungicides that protect crops from fungal diseases. Its structure enables effective disruption of ergosterol biosynthesis in fungi, making it valuable in developing plant protection agents. Also utilized in the preparation of pharmaceutical compounds where triazole rings contribute to biological activity, especially in antimicrobial and anti-inflammatory agents. Its trifluoromethyl and chloro functional groups enhance metabolic stability and lipophilicity, improving efficacy in agrochemical and medicinal applications.

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