(R)-tert-Butyl but-3-yn-2-ylcarbamate

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Reagent Code: #37762
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CAS Number 118080-82-3

science Other reagents with same CAS 118080-82-3

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Weight 169.2200 g/mol
Formula C₉H₁₅NO₂
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MDL Number MFCD18831560
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This compound is primarily used in organic synthesis as a chiral building block for the development of pharmaceuticals and biologically active molecules. Its structure, featuring a tert-butyl carbamate group and an alkyne moiety, makes it valuable for click chemistry reactions, particularly in the synthesis of complex molecules through copper-catalyzed azide-alkyne cycloaddition (CuAAC). It is also employed in the preparation of chiral intermediates for drug discovery, where its stereochemistry plays a critical role in the efficacy and specificity of the final product. Additionally, it serves as a protective group for amines in peptide synthesis, ensuring selective reactions during multi-step processes.

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inventory 250mg
10-20 days ฿1,359.00

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(R)-tert-Butyl but-3-yn-2-ylcarbamate
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This compound is primarily used in organic synthesis as a chiral building block for the development of pharmaceuticals and biologically active molecules. Its structure, featuring a tert-butyl carbamate group and an alkyne moiety, makes it valuable for click chemistry reactions, particularly in the synthesis of complex molecules through copper-catalyzed azide-alkyne cycloaddition (CuAAC). It is also employed in the preparation of chiral intermediates for drug discovery, where its stereochemistry plays a c

This compound is primarily used in organic synthesis as a chiral building block for the development of pharmaceuticals and biologically active molecules. Its structure, featuring a tert-butyl carbamate group and an alkyne moiety, makes it valuable for click chemistry reactions, particularly in the synthesis of complex molecules through copper-catalyzed azide-alkyne cycloaddition (CuAAC). It is also employed in the preparation of chiral intermediates for drug discovery, where its stereochemistry plays a critical role in the efficacy and specificity of the final product. Additionally, it serves as a protective group for amines in peptide synthesis, ensuring selective reactions during multi-step processes.

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