L-Methionine Allyl Ester Tosylate
≥95%
- Product Code: 105371
CAS:
142601-87-4
| Molecular Weight: | 361.48 g./mol | Molecular Formula: | C₁₅H₂₃NO₅S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00077939 | |
| Melting Point: | 114-116 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
L-Methionine Allyl Ester Tosylate finds its primary application in the field of organic synthesis, particularly in the production of peptides and other biologically active compounds. It serves as a key intermediate in the development of pharmaceuticals, enabling the introduction of methionine residues into peptide chains. This compound is also utilized in the synthesis of modified amino acids, which are essential for studying enzyme mechanisms and protein functions. Additionally, it plays a role in the preparation of prodrugs, where its ester functionality can be leveraged for controlled release of active pharmaceutical ingredients. In research, it is often employed as a building block for creating complex molecules with potential therapeutic applications. Its tosylate group enhances reactivity, making it a valuable reagent in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿16,983.00 |
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L-Methionine Allyl Ester Tosylate
L-Methionine Allyl Ester Tosylate finds its primary application in the field of organic synthesis, particularly in the production of peptides and other biologically active compounds. It serves as a key intermediate in the development of pharmaceuticals, enabling the introduction of methionine residues into peptide chains. This compound is also utilized in the synthesis of modified amino acids, which are essential for studying enzyme mechanisms and protein functions. Additionally, it plays a role in the preparation of prodrugs, where its ester functionality can be leveraged for controlled release of active pharmaceutical ingredients. In research, it is often employed as a building block for creating complex molecules with potential therapeutic applications. Its tosylate group enhances reactivity, making it a valuable reagent in various chemical transformations.
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