4-Ethyl-1H-pyrazol-3-amine

≥95%

Reagent Code: #184800
label
Alias 3-amino-4-ethylpyrazole
fingerprint
CAS Number 43024-15-3

science Other reagents with same CAS 43024-15-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 111.15 g/mol
Formula C₅H₉N₃
badge Registry Numbers
MDL Number MFCD06797570
thermostat Physical Properties
Boiling Point 307.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating novel pesticides with improved efficacy. Its structure supports the design of bioactive molecules due to the presence of both amine and heterocyclic functionalities, enabling diverse chemical modifications. Also employed in research for drug discovery targeting inflammatory and neurological disorders.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,150.00
250mg
10-20 days ฿4,900.00
500mg
10-20 days ฿9,600.00
1g
10-20 days ฿13,440.00
5g
10-20 days ฿40,000.00
10g
10-20 days ฿64,000.00
4-Ethyl-1H-pyrazol-3-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating novel pesticides with improved efficacy. Its structure supports the design of bioactive molecules due to the presence of both amine and heterocyclic functionalities, enabling diverse chemical modifications. Also employed in research for drug discovery targeting inflammatory and neurological disorders.
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals for creating novel pesticides with improved efficacy. Its structure supports the design of bioactive molecules due to the presence of both amine and heterocyclic functionalities, enabling diverse chemical modifications. Also employed in research for drug discovery targeting inflammatory and neurological disorders.
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