(S)-Diallyl 2-aminopentanedioate 4-methylbenzenesulfonate
98%
- Product Code: 104635
CAS:
20845-16-3
| Molecular Weight: | 399.46 g./mol | Molecular Formula: | C₁₈H₂₅NO₇S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00043307 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
(S)-Diallyl 2-aminopentanedioate 4-methylbenzenesulfonate is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure makes it a valuable building block for creating complex molecules, especially those with chiral centers, which are crucial in drug design. The compound is often employed in asymmetric synthesis to produce enantiomerically pure substances, enhancing the efficacy and safety of therapeutic agents. Additionally, it finds application in the preparation of biologically active compounds, including amino acid derivatives, which are essential in peptide synthesis and medicinal chemistry. Its role in facilitating selective reactions underscores its importance in advancing research and development in the pharmaceutical industry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Solid |
| Purity (%) | 97.5-100% |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | ฿7,002.00 |
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| 1g | 10-20 days | ฿2,007.00 |
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(S)-Diallyl 2-aminopentanedioate 4-methylbenzenesulfonate
(S)-Diallyl 2-aminopentanedioate 4-methylbenzenesulfonate is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure makes it a valuable building block for creating complex molecules, especially those with chiral centers, which are crucial in drug design. The compound is often employed in asymmetric synthesis to produce enantiomerically pure substances, enhancing the efficacy and safety of therapeutic agents. Additionally, it finds application in the preparation of biologically active compounds, including amino acid derivatives, which are essential in peptide synthesis and medicinal chemistry. Its role in facilitating selective reactions underscores its importance in advancing research and development in the pharmaceutical industry.
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