(R)-tert-Butyl but-3-yn-2-ylcarbamate
97%
- Product Code: 37762
CAS:
118080-82-3
| Molecular Weight: | 169.2200 g./mol | Molecular Formula: | C₉H₁₅NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18831560 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £30.74 |
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(R)-tert-Butyl but-3-yn-2-ylcarbamate
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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