(S)-2-Ethylbutyl 2-(((S)-(4-nitrophenoxy)(phenoxy)phosphoryl)amino)propanoate
99%
- Product Code: 38188
CAS:
1354823-36-1
Molecular Weight: | 450.42 g./mol | Molecular Formula: | C₂₁H₂₇N₂O₇P |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃, dry, airtight |
Product Description:
This chemical is primarily utilized in the synthesis of chiral compounds, particularly in the development of enantioselective catalysts and pharmaceuticals. Its structure, featuring chiral centers and a phosphoryl group, makes it valuable for creating optically active molecules. It is often employed in organic synthesis to introduce specific stereochemistry into target compounds, enhancing their biological activity or selectivity. Additionally, it can serve as an intermediate in the production of agrochemicals, where precise stereochemistry is crucial for efficacy. Its application extends to research settings, where it aids in studying enzyme interactions and designing inhibitors for therapeutic purposes.
Product Specification:
Test | Specification |
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APPEARANCE | solid |
PURITY | 98.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,800.00 |
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5.000 | 10-20 days | ฿5,600.00 |
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25.000 | 10-20 days | ฿19,980.00 |
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(S)-2-Ethylbutyl 2-(((S)-(4-nitrophenoxy)(phenoxy)phosphoryl)amino)propanoate
This chemical is primarily utilized in the synthesis of chiral compounds, particularly in the development of enantioselective catalysts and pharmaceuticals. Its structure, featuring chiral centers and a phosphoryl group, makes it valuable for creating optically active molecules. It is often employed in organic synthesis to introduce specific stereochemistry into target compounds, enhancing their biological activity or selectivity. Additionally, it can serve as an intermediate in the production of agrochemicals, where precise stereochemistry is crucial for efficacy. Its application extends to research settings, where it aids in studying enzyme interactions and designing inhibitors for therapeutic purposes.
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