tert-Butyl 3-amino-1H-pyrazole-1-carboxylate

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Reagent Code: #150276
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CAS Number 863504-84-1

science Other reagents with same CAS 863504-84-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.21 g/mol
Formula C₈H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD13194910
thermostat Physical Properties
Boiling Point 307 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine and heterocyclic structure make it valuable in medicinal chemistry for building nitrogen-containing rings found in drug candidates. Commonly employed in research settings for constructing pyrazole-based scaffolds that exhibit anti-inflammatory, antiviral, or anticancer activities. Also utilized in agrochemical research for designing novel active ingredients. Its stability and reactivity profile support use in multi-step organic syntheses, especially in coupling reactions and heterocycle formation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,430.00
inventory 5g
10-20 days ฿6,480.00
inventory 25g
10-20 days ฿32,210.00

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tert-Butyl 3-amino-1H-pyrazole-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine and heterocyclic structure make it valuable in medicinal chemistry for building nitrogen-containing rings found in drug candidates. Commonly employed in research settings for constructing pyrazole-based scaffolds that exhibit anti-inflammatory, antiviral, or anticancer activities. Also utilized in agrochemical research f

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine and heterocyclic structure make it valuable in medicinal chemistry for building nitrogen-containing rings found in drug candidates. Commonly employed in research settings for constructing pyrazole-based scaffolds that exhibit anti-inflammatory, antiviral, or anticancer activities. Also utilized in agrochemical research for designing novel active ingredients. Its stability and reactivity profile support use in multi-step organic syntheses, especially in coupling reactions and heterocycle formation.

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