(2S,4R)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid
98%
- Product Code: 87067
CAS:
1012341-54-6
Molecular Weight: | 383.48 g./mol | Molecular Formula: | C₂₃H₂₉NO₄ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its specific 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 is particularly useful for protecting the amine functionality during multi-step synthetic processes, ensuring selective reactions at other sites of the molecule. Additionally, the chiral centers in the compound allow for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects in therapeutic applications. Its application extends to research and development in medicinal chemistry, where it contributes to the design and optimization of new drug candidates targeting various diseases.
Product Specification:
Test | Specification |
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APPEARANCE | off White solid to white solid |
PURITY | 97.5-100 |
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 | Ft258,578.59 |
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0.250 | 10-20 days | Ft461,131.82 |
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(2S,4R)-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 specific 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 is particularly useful for protecting the amine functionality during multi-step synthetic processes, ensuring selective reactions at other sites of the molecule. Additionally, the chiral centers in the compound allow for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects in therapeutic applications. Its application extends to research and development in medicinal chemistry, where it contributes to the design and optimization of new drug candidates targeting various diseases.
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