3-Cyclopropyl-1H-pyrazole-5-carbohydrazide

95%

Reagent Code: #118102
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CAS Number 395653-63-1

science Other reagents with same CAS 395653-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.18 g/mol
Formula C₇H₁₀N₄O
badge Registry Numbers
MDL Number MFCD02163337
inventory_2 Storage & Handling
Density 1.426±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a cyclopropyl group and a pyrazole ring, makes it a valuable building block for developing compounds with potential therapeutic properties. Researchers often explore its derivatives for their antimicrobial, anti-inflammatory, and anticancer activities. Additionally, it is employed in the design of enzyme inhibitors, particularly targeting enzymes involved in disease pathways. Its versatility in chemical reactions also makes it useful in creating novel heterocyclic compounds for drug discovery and development.

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Test Parameter Specification
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿6,300.00

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3-Cyclopropyl-1H-pyrazole-5-carbohydrazide
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a cyclopropyl group and a pyrazole ring, makes it a valuable building block for developing compounds with potential therapeutic properties. Researchers often explore its derivatives for their antimicrobial, anti-inflammatory, and anticancer activities. Additionally, it is employed in the design
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a cyclopropyl group and a pyrazole ring, makes it a valuable building block for developing compounds with potential therapeutic properties. Researchers often explore its derivatives for their antimicrobial, anti-inflammatory, and anticancer activities. Additionally, it is employed in the design of enzyme inhibitors, particularly targeting enzymes involved in disease pathways. Its versatility in chemical reactions also makes it useful in creating novel heterocyclic compounds for drug discovery and development.
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