5-Amino-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile

≥95%

Reagent Code: #136925
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CAS Number 51516-67-7

science Other reagents with same CAS 51516-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.64 g/mol
Formula C₁₀H₇ClN₄
badge Registry Numbers
MDL Number MFCD00052031
thermostat Physical Properties
Boiling Point 424.2°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.41g/cm3
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active pyrazole derivatives, which exhibit anti-inflammatory, antimicrobial, and antitumor properties. Its nitrile and amino functional groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,190.00
inventory 5g
10-20 days ฿5,880.00

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5-Amino-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active pyrazole derivatives, which exhibit anti-inflammatory, antimicrobial, and antitumor properties. Its nitrile and amino functional groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also employed in agrochemical research for

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active pyrazole derivatives, which exhibit anti-inflammatory, antimicrobial, and antitumor properties. Its nitrile and amino functional groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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