tert-Butyl 4-amino-1H-pyrazole-1-carboxylate

≥95%

Reagent Code: #148687
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CAS Number 1018446-95-1

science Other reagents with same CAS 1018446-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.21 g/mol
Formula C₈H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD20697038
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Widely used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. The tert-butyl carboxylate serves as a protecting group for the pyrazole nitrogen, preventing tautomerism and enabling regioselective reactions in multi-step syntheses. This feature, combined with the free 4-amino group, makes it valuable in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders. The compound’s stability and reactivity profile support its use in combinatorial chemistry and high-throughput screening for new therapeutic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,000.00
inventory 1g
10-20 days ฿3,100.00
inventory 5g
10-20 days ฿12,590.00

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tert-Butyl 4-amino-1H-pyrazole-1-carboxylate
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Widely used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. The tert-butyl carboxylate serves as a protecting group for the pyrazole nitrogen, preventing tautomerism and enabling regioselective reactions in multi-step syntheses. This feature, combined with the free 4-amino group, makes it valuable in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders. The c

Widely used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. The tert-butyl carboxylate serves as a protecting group for the pyrazole nitrogen, preventing tautomerism and enabling regioselective reactions in multi-step syntheses. This feature, combined with the free 4-amino group, makes it valuable in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders. The compound’s stability and reactivity profile support its use in combinatorial chemistry and high-throughput screening for new therapeutic agents.

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