tert-Butyl ((3-bromopyridin-4-yl)methyl)carbamate

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Reagent Code: #36692
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CAS Number 1060813-11-7

science Other reagents with same CAS 1060813-11-7

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Weight 287.1530 g/mol
Formula C₁₁H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD13189515
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description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure, featuring a bromopyridine moiety and a carbamate group, makes it valuable for constructing complex molecules through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, it is employed in the development of inhibitors and modulators for biological targets, contributing to research in medicinal chemistry. Its stability and reactivity also make it suitable for use in peptide synthesis and as a protecting group in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,869.00

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tert-Butyl ((3-bromopyridin-4-yl)methyl)carbamate
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This chemical is primarily utilized in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure, featuring a bromopyridine moiety and a carbamate group, makes it valuable for constructing complex molecules through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, it is employed in the development of inhibitors an

This chemical is primarily utilized in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure, featuring a bromopyridine moiety and a carbamate group, makes it valuable for constructing complex molecules through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, it is employed in the development of inhibitors and modulators for biological targets, contributing to research in medicinal chemistry. Its stability and reactivity also make it suitable for use in peptide synthesis and as a protecting group in multi-step synthetic processes.

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