1-(4-(1H-Pyrazol-1-yl)phenyl)ethanamine

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Reagent Code: #197772
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CAS Number 866782-06-1

science Other reagents with same CAS 866782-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₁₁H₁₃N₃
badge Registry Numbers
MDL Number MFCD08572145
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used in pharmaceutical research as a key intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, making it valuable in drug discovery. Also employed in the preparation of pyrazole-containing derivatives with potential antitumor and antimicrobial properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and solubility in lead compounds.

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inventory 1g
10-20 days ฿32,100.00

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1-(4-(1H-Pyrazol-1-yl)phenyl)ethanamine
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Used in pharmaceutical research as a key intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, making it valuable in drug discovery. Also employed in the preparation of pyrazole-containing derivatives with potential antitumor and antimicrobial properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its abilit

Used in pharmaceutical research as a key intermediate for synthesizing biologically active compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, making it valuable in drug discovery. Also employed in the preparation of pyrazole-containing derivatives with potential antitumor and antimicrobial properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and solubility in lead compounds.

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