1-Methyl-5-(4-(trifluoromethyl)phenyl)-1H-pyrazole-4-carbaldehyde

98%

Reagent Code: #214070
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CAS Number 689250-58-6

science Other reagents with same CAS 689250-58-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.21 g/mol
Formula C₁₂H₉F₃N₂O
badge Registry Numbers
MDL Number MFCD21090877
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antitumor and anti-inflammatory properties. Its structure supports the construction of pyrazole-based derivatives that are explored in medicinal chemistry for their enzyme inhibitory effects. Also employed in agrochemical research for designing novel pesticides and fungicides due to the presence of trifluoromethyl group, which enhances metabolic stability and lipophilicity. Commonly utilized in organic synthesis for building complex heterocyclic systems through transformations at the aldehyde functional group.

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inventory 100mg
10-20 days ฿10,350.00

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1-Methyl-5-(4-(trifluoromethyl)phenyl)-1H-pyrazole-4-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antitumor and anti-inflammatory properties. Its structure supports the construction of pyrazole-based derivatives that are explored in medicinal chemistry for their enzyme inhibitory effects. Also employed in agrochemical research for designing novel pesticides and fungicides due to the presence of trifluoromethyl group, which enhances metabolic stability and lipophilicity

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antitumor and anti-inflammatory properties. Its structure supports the construction of pyrazole-based derivatives that are explored in medicinal chemistry for their enzyme inhibitory effects. Also employed in agrochemical research for designing novel pesticides and fungicides due to the presence of trifluoromethyl group, which enhances metabolic stability and lipophilicity. Commonly utilized in organic synthesis for building complex heterocyclic systems through transformations at the aldehyde functional group.

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