L-Glutamic acid dibenzyl ester 4-toluenesulfonate
98%
- Product Code: 105389
Alias:
L-glutamic acid dibenzyl ester p-toluenesulfonate
CAS:
2791-84-6
| Molecular Weight: | 499.58 g./mol | Molecular Formula: | C₂₆H₂₉N₂O₇S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
L-Glutamic acid dibenzyl ester 4-toluenesulfonate is primarily used in organic synthesis and peptide chemistry. It serves as a protected form of glutamic acid, allowing selective reactions to occur without affecting the amino or carboxyl groups. This compound is particularly valuable in the synthesis of peptides, where it helps in building complex structures by providing stability and control during the reaction process. Additionally, it is utilized in research and development for creating modified amino acids and exploring their biological activities. Its role in protecting functional groups makes it a key reagent in the preparation of specialized peptides and pharmaceutical intermediates.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿400.00 |
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| 25.000 | 10-20 days | ฿1,300.00 |
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| 100.000 | 10-20 days | ฿4,360.00 |
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| 500.000 | 10-20 days | ฿13,820.00 |
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L-Glutamic acid dibenzyl ester 4-toluenesulfonate
L-Glutamic acid dibenzyl ester 4-toluenesulfonate is primarily used in organic synthesis and peptide chemistry. It serves as a protected form of glutamic acid, allowing selective reactions to occur without affecting the amino or carboxyl groups. This compound is particularly valuable in the synthesis of peptides, where it helps in building complex structures by providing stability and control during the reaction process. Additionally, it is utilized in research and development for creating modified amino acids and exploring their biological activities. Its role in protecting functional groups makes it a key reagent in the preparation of specialized peptides and pharmaceutical intermediates.
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