(1-Phenyl-1H-pyrazol-3-yl)methanamine hydrochloride

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Reagent Code: #227097
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CAS Number 1170903-85-1

science Other reagents with same CAS 1170903-85-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.68 g/mol
Formula C₁₀H₁₂ClN₃
badge Registry Numbers
MDL Number MFCD12197097
inventory_2 Storage & Handling
Storage 2-8°C, Inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory, analgesic, and antipyretic properties. It serves as a building block in the preparation of pyrazole-based drug candidates, which are of interest in medicinal chemistry due to their biological activity and metabolic stability. Its amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, and other functional groups important in drug design. Commonly employed in research settings for structure-activity relationship (SAR) studies targeting central nervous system agents and kinase inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,480.00
inventory 250mg
10-20 days ฿5,680.00
inventory 1g
10-20 days ฿20,370.00

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(1-Phenyl-1H-pyrazol-3-yl)methanamine hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory, analgesic, and antipyretic properties. It serves as a building block in the preparation of pyrazole-based drug candidates, which are of interest in medicinal chemistry due to their biological activity and metabolic stability. Its amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, and other funct

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory, analgesic, and antipyretic properties. It serves as a building block in the preparation of pyrazole-based drug candidates, which are of interest in medicinal chemistry due to their biological activity and metabolic stability. Its amine functionality allows for easy derivatization, enabling the formation of amides, sulfonamides, and other functional groups important in drug design. Commonly employed in research settings for structure-activity relationship (SAR) studies targeting central nervous system agents and kinase inhibitors.

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