Boc-4,5-dehydro-leu-oh dcha
95%
- Product Code: 76496
CAS:
87720-54-5
Molecular Weight: | 410.59 g./mol | Molecular Formula: | C₂₃H₄₂N₂O₄ |
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EC Number: | MDL Number: | MFCD00237524 | |
Melting Point: | 148-153 °C | Boiling Point: | 365 °C at 760 mmHg |
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in peptide synthesis, this compound acts as a protected form of leucine, facilitating the controlled construction of peptide chains. Its application is crucial in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs where precise amino acid incorporation is required. The Boc (tert-butoxycarbonyl) protecting group ensures that the amino acid remains stable during the synthesis process, preventing unwanted side reactions. Additionally, the DCHA (dicyclohexylamine) salt form enhances the compound's solubility and handling properties, making it easier to work with in laboratory settings. This chemical is also employed in research focused on understanding protein structures and functions, as well as in the production of custom peptides for biochemical studies.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | £76.33 |
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0.250 | 10-20 days | £266.04 |
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1.000 | 10-20 days | £736.45 |
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Boc-4,5-dehydro-leu-oh dcha
Used primarily in peptide synthesis, this compound acts as a protected form of leucine, facilitating the controlled construction of peptide chains. Its application is crucial in the development of pharmaceuticals, particularly in the synthesis of peptide-based drugs where precise amino acid incorporation is required. The Boc (tert-butoxycarbonyl) protecting group ensures that the amino acid remains stable during the synthesis process, preventing unwanted side reactions. Additionally, the DCHA (dicyclohexylamine) salt form enhances the compound's solubility and handling properties, making it easier to work with in laboratory settings. This chemical is also employed in research focused on understanding protein structures and functions, as well as in the production of custom peptides for biochemical studies.
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