N-(p-Tolylsulphonyl)-L-glutamic acid
98%
- Product Code: 57974
Alias:
Tosylglutamic acid 2-(p-methylbenzenesulfonylamino)glutaric acid N-(4-methylbenzenesulfonyl)-L-glutamic acid N-(p-toluenesulfonyl)glutamic acid
CAS:
4816-80-2
| Molecular Weight: | 301.32 g./mol | Molecular Formula: | C₁₂H₁₅NO₆S |
|---|---|---|---|
| EC Number: | 225-390-1 | MDL Number: | MFCD00020545 |
| Melting Point: | 122-137°C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily used in biochemical research as a substrate or intermediate in enzymatic studies, particularly those involving glutamic acid metabolism. It serves as a model compound to investigate enzyme specificity and reaction mechanisms, especially in the context of sulfonamide derivatives. Additionally, it is utilized in the synthesis of more complex molecules, including peptides and pharmaceuticals, where its functional groups can be strategically modified. Its role in studying sulfonamide interactions also makes it relevant in the development of antimicrobial agents.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| Melting point | 122 137? |
| ACETATE | 20.5-23.5 |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿430.00 |
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| 25.000 | 10-20 days | ฿1,580.00 |
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| 100.000 | 10-20 days | ฿3,940.00 |
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| 500.000 | 10-20 days | ฿15,350.00 |
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N-(p-Tolylsulphonyl)-L-glutamic acid
This compound is primarily used in biochemical research as a substrate or intermediate in enzymatic studies, particularly those involving glutamic acid metabolism. It serves as a model compound to investigate enzyme specificity and reaction mechanisms, especially in the context of sulfonamide derivatives. Additionally, it is utilized in the synthesis of more complex molecules, including peptides and pharmaceuticals, where its functional groups can be strategically modified. Its role in studying sulfonamide interactions also makes it relevant in the development of antimicrobial agents.
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