Methyl 2-(2-(bromomethyl)phenyl)-2-(methoxyimino)acetate
95%
- Product Code: 62287
CAS:
115199-26-3
| Molecular Weight: | 286.12 g./mol | Molecular Formula: | C₁₁H₁₂BrNO₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 343.7±44.0 °C(Predicted) | |
| Density: | 1.38±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in the synthesis of various pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of cephalosporin antibiotics, which are widely used to treat bacterial infections. The presence of both the bromomethyl and methoxyimino groups allows for versatile chemical reactions, enabling the creation of complex molecular structures essential for drug development. Additionally, it is employed in organic synthesis for constructing nitrogen-containing heterocycles, which are crucial in the design of new therapeutic agents and crop protection chemicals. Its reactive sites make it valuable for cross-coupling reactions and functional group transformations in advanced chemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,474.00 |
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| 1.000 | 10-20 days | ฿8,883.00 |
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| 5.000 | 10-20 days | ฿32,148.00 |
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Methyl 2-(2-(bromomethyl)phenyl)-2-(methoxyimino)acetate
This compound is primarily utilized in the synthesis of various pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of cephalosporin antibiotics, which are widely used to treat bacterial infections. The presence of both the bromomethyl and methoxyimino groups allows for versatile chemical reactions, enabling the creation of complex molecular structures essential for drug development. Additionally, it is employed in organic synthesis for constructing nitrogen-containing heterocycles, which are crucial in the design of new therapeutic agents and crop protection chemicals. Its reactive sites make it valuable for cross-coupling reactions and functional group transformations in advanced chemical research.
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