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
25.000 10-20 days ฿560.00
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100.000 10-20 days ฿900.00
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500.000 10-20 days ฿2,880.00
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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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