(S)-(-)-1-(TERT-BUTOXYCARBONYL)-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE
98%
- Product Code: 37808
CAS:
119838-38-9
| Molecular Weight: | 256.34 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075101 | |
| Melting Point: | 67-69℃(lit.) | Boiling Point: | 355.3℃ at 760 mmHg |
| Density: | 1.064±0.06g/ml(Predicted) | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is widely utilized in organic synthesis as a chiral auxiliary or building block for the preparation of complex molecules, particularly in the pharmaceutical industry. It is often employed in asymmetric synthesis to induce stereoselectivity, enabling the production of enantiomerically pure compounds. Its tert-butoxycarbonyl (Boc) protecting group is particularly valuable in peptide synthesis, where it safeguards amine functionalities during reactions. Additionally, its rigid imidazolidinone structure makes it useful in the development of catalysts and ligands for asymmetric transformations, enhancing the efficiency and selectivity of chemical reactions. Its application extends to the synthesis of biologically active compounds, including drug candidates and natural products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $196.97 |
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| 1.000 | 10-20 days | $569.99 |
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(S)-(-)-1-(TERT-BUTOXYCARBONYL)-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE
This chemical is widely utilized in organic synthesis as a chiral auxiliary or building block for the preparation of complex molecules, particularly in the pharmaceutical industry. It is often employed in asymmetric synthesis to induce stereoselectivity, enabling the production of enantiomerically pure compounds. Its tert-butoxycarbonyl (Boc) protecting group is particularly valuable in peptide synthesis, where it safeguards amine functionalities during reactions. Additionally, its rigid imidazolidinone structure makes it useful in the development of catalysts and ligands for asymmetric transformations, enhancing the efficiency and selectivity of chemical reactions. Its application extends to the synthesis of biologically active compounds, including drug candidates and natural products.
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