CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
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  • CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
  • CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
  • CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
  • CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
  • CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
  • CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide
  • CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide

CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide

CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide MF:C8H7BrFNO MW:232.05 EINECS:600-141-3 Appearance:WHITE SOLID Puity:97%min COA:Provide

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Life Science Chemicals

Pharmaceutical Intermediates

Product introduction

PRODUCT NAME 2'-Bromo-4'-fluoroacetanilide
CAS NO 1009-22-9 
MP 117-119 °C(lit.)
BP 337.5±32.0 °C(Predicted)
DENSITY 1.623±0.06 g/cm3(Predicted)
STORAGE 2-8°C
DELIVERY 2-3DAYS
PACKAGE According client's request

Description of CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide

2'-Bromo-4'-fluoroacetanilide CAS NO:1009-22-9 is a synthetic derivative of acetanilide that is used in the treatment of diabetes mellitus. It has been shown to have antidiabetic properties as well as to inhibit the formation of nitrosamines, which are carcinogenic compounds. The synthesis of 2'-bromo-4'-fluoroacetanilide involves the addition of bromine and sodium hydrogen to acetylated acetanilide. This reaction occurs in a reaction vessel at an elevated temperature, with the solvent being an organic solvent. The final product is isolated by distillation and purified by recrystallization or column chromatography. Molecular docking analysis has shown that 2'-bromo-4'-fluoroacetanilide binds to ATP synthase, which is involved in gluconeogenesis and glycolysis, leading to its ability to inhibit glucose production in cells.

 

 


Applications of CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide


Chemistry: Used as an intermediate in the synthesis of various organic compounds.

Biology: Employed in the study of enzyme inhibition and protein interactions.

Medicine: Investigated for its potential therapeutic properties, including anti-inflammatory and anticancer activities.

Industry: Utilized in the production of pharmaceuticals, agrochemicals, and specialty chemicals.
 

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CAS NO:1009-22-9 2'-Bromo-4'-fluoroacetanilide

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