(1-Methyl-5-phenoxy-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanol

≥95%

Reagent Code: #214346
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CAS Number 318469-22-6

science Other reagents with same CAS 318469-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.22 g/mol
Formula C₁₂H₁₁F₃N₂O₂
badge Registry Numbers
MDL Number MFCD00172652
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the design of molecules with enhanced metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for optimizing lead compounds due to the presence of trifluoromethyl and phenoxy groups, which improve lipophilicity and bioavailability. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and environmental profiles.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿21,730.00
inventory 1g
10-20 days ฿34,960.00

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(1-Methyl-5-phenoxy-3-(trifluoromethyl)-1H-pyrazol-4-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the design of molecules with enhanced metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for optimizing lead compounds due to the presence of trifluoromethyl and phenoxy groups, which improve lipophilicity and bioavailability. Also utilized in agrochemical research for develo

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the design of molecules with enhanced metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for optimizing lead compounds due to the presence of trifluoromethyl and phenoxy groups, which improve lipophilicity and bioavailability. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and environmental profiles.

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