tert-Butyl (2-chloro-5-formylpyridin-4-yl)carbamate

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Reagent Code: #141580
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CAS Number 1956381-87-5

science Other reagents with same CAS 1956381-87-5

blur_circular Chemical Specifications

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Weight 256.69 g/mol
Formula C₁₁H₁₃ClN₂O₃
badge Registry Numbers
MDL Number MFCD29059300
inventory_2 Storage & Handling
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. The aldehyde group allows for further functionalization through reactions such as reductive amination or Wittig-type transformations, enabling the introduction of diverse side chains. The tert-butyloxycarbonyl (Boc) protecting group stabilizes the amine during synthetic steps and can be selectively removed under acidic conditions, making this compound valuable in multi-step organic synthesis. Its pyridine core contributes to enhanced binding affinity in drug candidates targeting enzymes and receptors involved in inflammatory and oncological pathways.

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inventory 100mg
10-20 days ฿16,930.00

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tert-Butyl (2-chloro-5-formylpyridin-4-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. The aldehyde group allows for further functionalization through reactions such as reductive amination or Wittig-type transformations, enabling the introduction of diverse side chains. The tert-butyloxycarbonyl (Boc) protecting group stabilizes the amine during synthetic steps and can be selectively removed under acidic conditions, making this

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The aldehyde group allows for further functionalization through reactions such as reductive amination or Wittig-type transformations, enabling the introduction of diverse side chains. The tert-butyloxycarbonyl (Boc) protecting group stabilizes the amine during synthetic steps and can be selectively removed under acidic conditions, making this compound valuable in multi-step organic synthesis. Its pyridine core contributes to enhanced binding affinity in drug candidates targeting enzymes and receptors involved in inflammatory and oncological pathways.

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