(2R,4S)-5-([1,1'-Biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid
≥95%
- Product Code: 104134
CAS:
1012341-50-2
Molecular Weight: | 383.48 g./mol | Molecular Formula: | C₂₃H₂₉NO₄ |
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EC Number: | MDL Number: | MFCD27955981 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its structure, featuring a biphenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of protease inhibitors and other biologically active compounds. The Boc group serves as a protective moiety during synthetic processes, ensuring selective reactivity and stability. Additionally, the chiral centers in the molecule allow for the creation of enantiomerically pure substances, which is critical in designing drugs with specific therapeutic effects and reduced side effects. Its application is particularly relevant in the production of targeted therapies for diseases such as cancer and viral infections.
Product Specification:
Test | Specification |
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Appearance | White To Off-White Powder Or Crystals |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $13.37 |
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0.250 | 10-20 days | $18.09 |
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1.000 | 10-20 days | $53.48 |
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5.000 | 10-20 days | $218.65 |
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25.000 | 10-20 days | $990.23 |
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(2R,4S)-5-([1,1'-Biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its structure, featuring a biphenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of protease inhibitors and other biologically active compounds. The Boc group serves as a protective moiety during synthetic processes, ensuring selective reactivity and stability. Additionally, the chiral centers in the molecule allow for the creation of enantiomerically pure substances, which is critical in designing drugs with specific therapeutic effects and reduced side effects. Its application is particularly relevant in the production of targeted therapies for diseases such as cancer and viral infections.
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