(S)-2-((tert-Butoxycarbonyl)amino)hexanedioic acid
≥95%
- Product Code: 54182
CAS:
77302-72-8
| Molecular Weight: | 261.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00063354 | |
| Melting Point: | Boiling Point: | 462.1°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a crucial building block in the preparation of biologically active molecules, particularly in the development of drugs targeting specific enzymes or receptors. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during peptide synthesis, enhancing the efficiency of the process. Additionally, it is employed in the production of chiral compounds, leveraging its stereochemistry to create enantiomerically pure substances for therapeutic applications. Its role in organic synthesis also extends to the creation of complex organic molecules used in research and drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿10,107.00 |
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| 5g | 10-20 days | ฿30,321.00 |
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| 250mg | 10-20 days | ฿4,302.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)hexanedioic acid
This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a crucial building block in the preparation of biologically active molecules, particularly in the development of drugs targeting specific enzymes or receptors. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during peptide synthesis, enhancing the efficiency of the process. Additionally, it is employed in the production of chiral compounds, leveraging its stereochemistry to create enantiomerically pure substances for therapeutic applications. Its role in organic synthesis also extends to the creation of complex organic molecules used in research and drug discovery.
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