(R)-3-((tert-Butoxycarbonyl)amino)-3-(2-chlorophenyl)propanoic acid
98%
- Product Code: 104252
CAS:
500789-05-9
Molecular Weight: | 299.75 g./mol | Molecular Formula: | C₁₄H₁₈ClNO₄ |
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EC Number: | MDL Number: | MFCD03427958 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it valuable for constructing chiral compounds, which are essential in the production of enantiomerically pure drugs. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molecule. Additionally, the presence of the chlorophenyl group can enhance binding affinity to specific biological targets, making it useful in the design of receptor-specific drugs. Its application is often seen in the development of therapeutic agents targeting neurological disorders, cardiovascular diseases, or other conditions where chiral specificity is critical.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,610.00 |
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0.250 | 10-20 days | ฿3,870.00 |
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1.000 | 10-20 days | ฿9,720.00 |
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(R)-3-((tert-Butoxycarbonyl)amino)-3-(2-chlorophenyl)propanoic acid
This compound is primarily utilized in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it valuable for constructing chiral compounds, which are essential in the production of enantiomerically pure drugs. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molecule. Additionally, the presence of the chlorophenyl group can enhance binding affinity to specific biological targets, making it useful in the design of receptor-specific drugs. Its application is often seen in the development of therapeutic agents targeting neurological disorders, cardiovascular diseases, or other conditions where chiral specificity is critical.
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