Tert-Butyl 2-Bromo-2-(Diethoxyphosphoryl)Acetate
95%
- Product Code: 66846
CAS:
179106-93-5
| Molecular Weight: | 331.14 g./mol | Molecular Formula: | C₁₀H₂₀BrO₅P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD25960184 | |
| Melting Point: | Boiling Point: | 339.2±32.0 °C(Predicted) | |
| Density: | 1.337±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various biologically active molecules. It is particularly valuable in the construction of complex organic frameworks, especially in the synthesis of phosphonate esters, which are crucial in medicinal chemistry and agrochemical development. Its reactive bromine and phosphonate groups make it a versatile building block for cross-coupling reactions, enabling the formation of carbon-carbon and carbon-phosphorus bonds. Additionally, it finds application in the development of protease inhibitors and other enzyme-targeting drugs, owing to its ability to mimic phosphate groups in biological systems. Its use in asymmetric synthesis also contributes to the production of chiral compounds, which are essential in the pharmaceutical industry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft63,998.20 |
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| 0.250 | 10-20 days | Ft116,360.37 |
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| 1.000 | 10-20 days | Ft232,720.73 |
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Tert-Butyl 2-Bromo-2-(Diethoxyphosphoryl)Acetate
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various biologically active molecules. It is particularly valuable in the construction of complex organic frameworks, especially in the synthesis of phosphonate esters, which are crucial in medicinal chemistry and agrochemical development. Its reactive bromine and phosphonate groups make it a versatile building block for cross-coupling reactions, enabling the formation of carbon-carbon and carbon-phosphorus bonds. Additionally, it finds application in the development of protease inhibitors and other enzyme-targeting drugs, owing to its ability to mimic phosphate groups in biological systems. Its use in asymmetric synthesis also contributes to the production of chiral compounds, which are essential in the pharmaceutical industry.
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