tert-Butyl (2-chloro-5-fluoropyridin-3-yl)carbamate

95%

Reagent Code: #131329
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CAS Number 1394899-03-6

science Other reagents with same CAS 1394899-03-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.67 g/mol
Formula C₁₀H₁₂ClFN₂O₂
badge Registry Numbers
MDL Number MFCD22392295
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization in drug design, making it valuable in medicinal chemistry for creating analogs with improved potency and metabolic stability. Commonly employed in agrochemical research as well, where it contributes to the creation of novel pesticides and herbicides with enhanced environmental profiles. The tert-butyl carbamate group acts as a protecting group for amines during multi-step syntheses, enabling controlled deprotection under mild acidic conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,170.00
inventory 250mg
10-20 days ฿14,180.00

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tert-Butyl (2-chloro-5-fluoropyridin-3-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 bioactive molecules. Its structure allows for selective functionalization in drug design, making it valuable in medicinal chemistry for creating analogs with improved potency and metabolic stability. Commonly employed in agrochemical research as well, where it contributes to the creation of novel pesticides and herbicides with enhanced environmental profiles. The tert-butyl

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization in drug design, making it valuable in medicinal chemistry for creating analogs with improved potency and metabolic stability. Commonly employed in agrochemical research as well, where it contributes to the creation of novel pesticides and herbicides with enhanced environmental profiles. The tert-butyl carbamate group acts as a protecting group for amines during multi-step syntheses, enabling controlled deprotection under mild acidic conditions.

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