(R)-3-((tert-Butoxycarbonyl)amino)-3-(4-cyanophenyl)propanoic acid
≥98% (HPLC)
- Product Code: 104253
Alias:
(R)-Boc-4-cyano-β-Phe-OH
CAS:
501015-22-1
Molecular Weight: | 290.31 g./mol | Molecular Formula: | C₁₅H₁₈N₂O₄ |
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EC Number: | MDL Number: | MFCD03427968 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a cyano functional group, makes it particularly valuable in the development of peptide-based drugs and other bioactive compounds. The Boc group is often employed to protect amines during synthesis, ensuring selective reactions, while the cyano group can serve as a precursor for further chemical transformations, such as conversion to carboxylic acids or amides. Its application is significant in the design and production of therapeutic agents targeting various diseases, including neurological disorders and cancer. Additionally, its chiral center allows for the creation of enantiomerically pure substances, which is crucial for optimizing drug efficacy and reducing side effects.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,390.00 |
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0.500 | 10-20 days | ฿11,000.00 |
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(R)-3-((tert-Butoxycarbonyl)amino)-3-(4-cyanophenyl)propanoic acid
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a cyano functional group, makes it particularly valuable in the development of peptide-based drugs and other bioactive compounds. The Boc group is often employed to protect amines during synthesis, ensuring selective reactions, while the cyano group can serve as a precursor for further chemical transformations, such as conversion to carboxylic acids or amides. Its application is significant in the design and production of therapeutic agents targeting various diseases, including neurological disorders and cancer. Additionally, its chiral center allows for the creation of enantiomerically pure substances, which is crucial for optimizing drug efficacy and reducing side effects.
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