(3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methanol

≥95%

Reagent Code: #180311
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CAS Number 58789-53-0

science Other reagents with same CAS 58789-53-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.25 g/mol
Formula C₁₂H₁₄N₂O
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MDL Number MFCD06202725
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of pyrazole-based drugs with anti-inflammatory and analgesic properties. Its hydroxyl group allows for easy functionalization, enabling the formation of esters, ethers, or conjugates to improve drug solubility or bioavailability. Also employed in the preparation of agrochemicals and biologically active molecules where the pyrazole scaffold plays a central role in target binding. Its structural features make it valuable in medicinal chemistry research for optimizing lead compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,880.00
inventory 1g
10-20 days ฿20,210.00

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(3,5-Dimethyl-1-phenyl-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 pyrazole-based drugs with anti-inflammatory and analgesic properties. Its hydroxyl group allows for easy functionalization, enabling the formation of esters, ethers, or conjugates to improve drug solubility or bioavailability. Also employed in the preparation of agrochemicals and biologically active molecules where the pyrazole scaffold plays a central role in target binding. Its structural features m

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of pyrazole-based drugs with anti-inflammatory and analgesic properties. Its hydroxyl group allows for easy functionalization, enabling the formation of esters, ethers, or conjugates to improve drug solubility or bioavailability. Also employed in the preparation of agrochemicals and biologically active molecules where the pyrazole scaffold plays a central role in target binding. Its structural features make it valuable in medicinal chemistry research for optimizing lead compounds.

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