4-[(tert-butoxycarbonyl)amino]-1-methyl-1H-pyrazole-3-carboxylicacid

98%

Reagent Code: #197610
fingerprint
CAS Number 1287670-05-6

science Other reagents with same CAS 1287670-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.24 g/mol
Formula C₁₀H₁₅N₃O₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of pyrazole-based scaffolds found in anti-inflammatory, anticancer, and antiviral agents. The carboxylic acid functionality enables coupling reactions with amines or alcohols to form amides or esters, facilitating structural diversification in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,920.00
inventory 1g
10-20 days ฿66,560.00
inventory 250mg
10-20 days ฿32,920.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-[(tert-butoxycarbonyl)amino]-1-methyl-1H-pyrazole-3-carboxylicacid
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of pyrazole-based scaffolds found in anti-inflammatory, anticancer, and antiviral agents. The carboxylic acid functionality enables coupling reactions with amines or alcohols to fo

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of pyrazole-based scaffolds found in anti-inflammatory, anticancer, and antiviral agents. The carboxylic acid functionality enables coupling reactions with amines or alcohols to form amides or esters, facilitating structural diversification in medicinal chemistry.

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...