1-Ethyl-1H-pyrazole-4-carbohydrazide

95%

Reagent Code: #185291
fingerprint
CAS Number 512809-51-7

science Other reagents with same CAS 512809-51-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.17 g/mol
Formula C₆H₁₀N₄O
badge Registry Numbers
MDL Number MFCD03419413
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive compounds and pharmaceuticals. It serves as a building block for heterocyclic compounds due to the presence of both pyrazole and hydrazide functional groups, which are common in medicinal chemistry. The hydrazide moiety enables reactions with aldehydes or ketones to form Schiff bases with potential pharmaceutical applications. Commonly employed in the development of antimicrobial, anti-inflammatory, and anticancer agents. Also utilized in agrochemical synthesis for creating novel pesticides and plant growth regulators. Additionally, it acts as a ligand for transition metal coordination complexes, which may be applied in catalysis or advanced materials. Its reactivity facilitates easy modification into derivatives for structure-activity relationship studies in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿860.00
inventory 250mg
10-20 days ฿1,970.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Ethyl-1H-pyrazole-4-carbohydrazide
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive compounds and pharmaceuticals. It serves as a building block for heterocyclic compounds due to the presence of both pyrazole and hydrazide functional groups, which are common in medicinal chemistry. The hydrazide moiety enables reactions with aldehydes or ketones to form Schiff bases with potential pharmaceutical applications. Commonly employed in the development of antimicrobial, anti-inflammatory, and anticancer

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive compounds and pharmaceuticals. It serves as a building block for heterocyclic compounds due to the presence of both pyrazole and hydrazide functional groups, which are common in medicinal chemistry. The hydrazide moiety enables reactions with aldehydes or ketones to form Schiff bases with potential pharmaceutical applications. Commonly employed in the development of antimicrobial, anti-inflammatory, and anticancer agents. Also utilized in agrochemical synthesis for creating novel pesticides and plant growth regulators. Additionally, it acts as a ligand for transition metal coordination complexes, which may be applied in catalysis or advanced materials. Its reactivity facilitates easy modification into derivatives for structure-activity relationship studies in drug discovery.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...