(E)-2-(2-bromophenyl)-N'-hydroxyacetimidamide
95%
- Product Code: 86336
CAS:
89980-71-2
| Molecular Weight: | 229.07 g./mol | Molecular Formula: | C₈H₉BrN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09808455 | |
| Melting Point: | 128-130 °C | Boiling Point: | 334.7±44.0 °C(Predicted) |
| Density: | 1.58±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the preparation of various heterocyclic compounds. Its structure, featuring a bromophenyl group and a hydroxyacetimidamide moiety, makes it a valuable building block for the development of pharmaceuticals and agrochemicals. Specifically, it is often employed in the synthesis of oxadiazoles and other nitrogen-containing heterocycles, which are known for their biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, its reactive functional groups allow for further chemical modifications, enabling the creation of diverse molecular frameworks for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $280.83 |
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| 0.250 | 10-20 days | $526.55 |
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| 1.000 | 10-20 days | $1,053.11 |
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(E)-2-(2-bromophenyl)-N'-hydroxyacetimidamide
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the preparation of various heterocyclic compounds. Its structure, featuring a bromophenyl group and a hydroxyacetimidamide moiety, makes it a valuable building block for the development of pharmaceuticals and agrochemicals. Specifically, it is often employed in the synthesis of oxadiazoles and other nitrogen-containing heterocycles, which are known for their biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, its reactive functional groups allow for further chemical modifications, enabling the creation of diverse molecular frameworks for drug discovery and development.
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