tert-Butyl 4-(4-chloro-1H-pyrazol-1-yl)piperidine-1-carboxylate

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Reagent Code: #152026
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CAS Number 1501970-55-3

science Other reagents with same CAS 1501970-55-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.77 g/mol
Formula C₁₃H₂₀ClN₃O₂
badge Registry Numbers
MDL Number MFCD29044339
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective modification in drug design, making it valuable in creating agents targeting inflammation, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides stability during synthesis and enables controlled deprotection for further functionalization. The chloropyrazole moiety contributes to binding affinity in various enzymatic assays, enhancing its utility in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,360.00
inventory 250mg
10-20 days ฿4,840.00
inventory 1g
10-20 days ฿15,610.00

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tert-Butyl 4-(4-chloro-1H-pyrazol-1-yl)piperidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective modification in drug design, making it valuable in creating agents targeting inflammation, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides stability during synthesis and enables controlled deprotection for further functionalization. The chloropyrazole moiety contributes to binding a

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective modification in drug design, making it valuable in creating agents targeting inflammation, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides stability during synthesis and enables controlled deprotection for further functionalization. The chloropyrazole moiety contributes to binding affinity in various enzymatic assays, enhancing its utility in medicinal chemistry research.

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