(S)-tert-Butyl 2-amino-2-phenylacetate
97%
- Product Code: 50228
CAS:
53934-78-4
Molecular Weight: | 207.27 g./mol | Molecular Formula: | C₁₂H₁₇NO₂ |
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EC Number: | MDL Number: | MFCD00238136 | |
Melting Point: | Boiling Point: | 280.2°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily used in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. It serves as an intermediate in the production of enantiomerically pure compounds, which are crucial for developing medications with higher efficacy and fewer side effects. Its chiral nature makes it valuable in asymmetric synthesis, particularly in creating active pharmaceutical ingredients (APIs) for treatments targeting neurological disorders, cardiovascular diseases, and infections. Additionally, it is employed in research and development for designing and testing new drug candidates, leveraging its structural properties to optimize molecular interactions and therapeutic outcomes.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white powder or crystals |
PURITY | 96.5-100 |
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 | ฿460.00 |
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1.000 | 10-20 days | ฿3,040.00 |
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5.000 | 10-20 days | ฿12,880.00 |
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(S)-tert-Butyl 2-amino-2-phenylacetate
This chemical is primarily used in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. It serves as an intermediate in the production of enantiomerically pure compounds, which are crucial for developing medications with higher efficacy and fewer side effects. Its chiral nature makes it valuable in asymmetric synthesis, particularly in creating active pharmaceutical ingredients (APIs) for treatments targeting neurological disorders, cardiovascular diseases, and infections. Additionally, it is employed in research and development for designing and testing new drug candidates, leveraging its structural properties to optimize molecular interactions and therapeutic outcomes.
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