tert-Butyl (2-bromo-6-chloropyridin-3-yl)carbamate

96%

Reagent Code: #113129
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CAS Number 1227958-32-8

science Other reagents with same CAS 1227958-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.57 g/mol
Formula C₁₀H₁₂BrClN₂O₂
badge Registry Numbers
MDL Number MFCD20039978
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring both a bromo and chloro substituent on the pyridine ring, makes it a versatile building block in pharmaceutical and agrochemical research. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine moieties into target molecules. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule. Its applications are particularly significant in the synthesis of active pharmaceutical ingredients (APIs) and biologically active compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿12,636.00
250mg
10-20 days ฿1,233.00
1g
10-20 days ฿3,249.00
100mg
10-20 days ฿684.00
tert-Butyl (2-bromo-6-chloropyridin-3-yl)carbamate
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This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring both a bromo and chloro substituent on the pyridine ring, makes it a versatile building block in pharmaceutical and agrochemical research. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine moieties into target molecules. Additionally, the tert-butyl carbamate group serves as a prot

This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring both a bromo and chloro substituent on the pyridine ring, makes it a versatile building block in pharmaceutical and agrochemical research. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine moieties into target molecules. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule. Its applications are particularly significant in the synthesis of active pharmaceutical ingredients (APIs) and biologically active compounds.

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