(5-Chloro-1-methyl-3-phenyl-1H-pyrazol-4-yl)(thiophen-2-yl)methanol

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Reagent Code: #156961
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CAS Number 29939-18-2

science Other reagents with same CAS 29939-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.8 g/mol
Formula C₁₅H₁₃ClN₂OS
badge Registry Numbers
MDL Number MFCD00664938
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the design of molecules with enhanced selectivity and binding affinity toward cyclooxygenase (COX) enzymes, making it valuable in the creation of non-steroidal anti-inflammatory drugs (NSAIDs). Additionally, it serves as a building block in medicinal chemistry for optimizing drug candidates with improved metabolic stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,060.00
inventory 250mg
10-20 days ฿18,790.00
inventory 1g
10-20 days ฿50,730.00

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(5-Chloro-1-methyl-3-phenyl-1H-pyrazol-4-yl)(thiophen-2-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 analgesic compounds. Its structure supports the design of molecules with enhanced selectivity and binding affinity toward cyclooxygenase (COX) enzymes, making it valuable in the creation of non-steroidal anti-inflammatory drugs (NSAIDs). Additionally, it serves as a building block in medicinal chemistry for optimizing drug candidates with improved metabolic stability and bioavail

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the design of molecules with enhanced selectivity and binding affinity toward cyclooxygenase (COX) enzymes, making it valuable in the creation of non-steroidal anti-inflammatory drugs (NSAIDs). Additionally, it serves as a building block in medicinal chemistry for optimizing drug candidates with improved metabolic stability and bioavailability.

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