tert-Butyl ((5-bromopyridin-2-yl)methyl)carbamate

98%

Reagent Code: #146085
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CAS Number 1188477-11-3

science Other reagents with same CAS 1188477-11-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.15 g/mol
Formula C₁₁H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD11520868
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling carbon–carbon bond formation. The tert-butyl carbamate (Boc) group serves as a protected amine, facilitating stepwise synthesis in peptide and peptidomimetic chemistry. Stable under various reaction conditions, it supports multi-step synthetic routes in drug discovery and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿850.00
inventory 250mg
10-20 days ฿1,370.00
inventory 1g
10-20 days ฿4,000.00
inventory 5g
10-20 days ฿15,730.00
inventory 25g
10-20 days ฿59,750.00

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tert-Butyl ((5-bromopyridin-2-yl)methyl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling carbon–carbon bond formation. The tert-butyl carbamate (Boc) group serves as a protected amine, facilitating stepwise synthesis in peptide and peptido

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions due to the presence of the bromo substituent, enabling carbon–carbon bond formation. The tert-butyl carbamate (Boc) group serves as a protected amine, facilitating stepwise synthesis in peptide and peptidomimetic chemistry. Stable under various reaction conditions, it supports multi-step synthetic routes in drug discovery and medicinal chemistry.

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