L-Tyrosine benzyl ester p-toluenesulfonate salt
98%
- Product Code: 105411
Alias:
L-tyrosine benzyl ester p-toluenesulfonate
CAS:
53587-11-4
| Molecular Weight: | 443.51 g./mol | Molecular Formula: | C₂₃H₂₅NO₆S |
|---|---|---|---|
| EC Number: | 258-650-8 | MDL Number: | MFCD00038959 |
| Melting Point: | 177 °C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
L-Tyrosine benzyl ester p-toluenesulfonate salt is primarily used in peptide synthesis as a protected form of tyrosine. The benzyl ester group protects the carboxylic acid functionality, while the p-toluenesulfonate salt enhances solubility and stability. This compound is particularly valuable in solid-phase peptide synthesis, where it allows for the controlled incorporation of tyrosine into peptide chains without unwanted side reactions. Additionally, it is utilized in research to study enzyme-substrate interactions and in the development of pharmaceuticals targeting tyrosine-related pathways. Its protective groups can be selectively removed under mild conditions, making it a versatile intermediate in organic and medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿500.00 |
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| 25.000 | 10-20 days | ฿2,200.00 |
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| 100.000 | 10-20 days | ฿6,500.00 |
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L-Tyrosine benzyl ester p-toluenesulfonate salt
L-Tyrosine benzyl ester p-toluenesulfonate salt is primarily used in peptide synthesis as a protected form of tyrosine. The benzyl ester group protects the carboxylic acid functionality, while the p-toluenesulfonate salt enhances solubility and stability. This compound is particularly valuable in solid-phase peptide synthesis, where it allows for the controlled incorporation of tyrosine into peptide chains without unwanted side reactions. Additionally, it is utilized in research to study enzyme-substrate interactions and in the development of pharmaceuticals targeting tyrosine-related pathways. Its protective groups can be selectively removed under mild conditions, making it a versatile intermediate in organic and medicinal chemistry.
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