Tert-Butyl (3-chloro-1-methyl-1H-pyrazol-5-yl)carbamate

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Reagent Code: #238162
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CAS Number 1312949-21-5

science Other reagents with same CAS 1312949-21-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.67 g/mol
Formula C₉H₁₄N₃O₂Cl
badge Registry Numbers
MDL Number MFCD22573940
thermostat Physical Properties
Boiling Point 281.9±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

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 structure allows for selective modification in drug design, improving metabolic stability and bioavailability. Commonly employed in agrochemical research for creating novel pesticides and herbicides due to its reactivity and functional group compatibility. Also utilized in medicinal chemistry for protecting amine groups during multi-step syntheses, enabling controlled reactions without interference from reactive nitrogen sites.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,610.00
inventory 1g
10-20 days ฿34,820.00

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Tert-Butyl (3-chloro-1-methyl-1H-pyrazol-5-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, improving metabolic stability and bioavailability. Commonly employed in agrochemical research for creating novel pesticides and herbicides due to its reactivity and functional group compatibility. Also utilized in medicinal chemistry for protecting amine groups during multi-step s

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, improving metabolic stability and bioavailability. Commonly employed in agrochemical research for creating novel pesticides and herbicides due to its reactivity and functional group compatibility. Also utilized in medicinal chemistry for protecting amine groups during multi-step syntheses, enabling controlled reactions without interference from reactive nitrogen sites.

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