5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide compound with 2-aminoethanol (1:1)
97%
- Product Code: 122806
CAS:
1420-04-8
| Molecular Weight: | 388.20 g./mol | Molecular Formula: | C₁₅H₁₅Cl₂N₃O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01941566 | |
| Melting Point: | Boiling Point: | 424.5°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the synthesis of advanced chemical intermediates, particularly in the development of pharmaceutical agents. Its structure allows it to act as a key building block in the creation of compounds with potential biological activity, such as antimicrobial or anti-inflammatory agents. The presence of both chloro and nitro groups enhances its reactivity, making it suitable for further chemical modifications. Additionally, it is employed in research settings to study structure-activity relationships, aiding in the design of new drugs. Its combination with 2-aminoethanol improves solubility and stability, facilitating its use in various experimental and industrial processes.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Pale-yellow To Yellow-brown Solid |
| 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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| 25.000 | 10-20 days | £12.67 |
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| 100.000 | 10-20 days | £20.36 |
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| 500.000 | 10-20 days | £65.14 |
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5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide compound with 2-aminoethanol (1:1)
This compound is primarily utilized in the synthesis of advanced chemical intermediates, particularly in the development of pharmaceutical agents. Its structure allows it to act as a key building block in the creation of compounds with potential biological activity, such as antimicrobial or anti-inflammatory agents. The presence of both chloro and nitro groups enhances its reactivity, making it suitable for further chemical modifications. Additionally, it is employed in research settings to study structure-activity relationships, aiding in the design of new drugs. Its combination with 2-aminoethanol improves solubility and stability, facilitating its use in various experimental and industrial processes.
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