chem
English Synonyms(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone;Methanone,(2-chloro-5-iodophenyl)(4-fluorophenyl)-;(2-Chloro-5-iodobenyl)(4-fluorophenyl)methanone;EmpagliflozinImpurity48;EnglenetImpurity16;2-chloro-4-fluoro-5-Iodobenzophenon;(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanon;2-Chloro-
915095-86-2
C13H7ClFIO
360.55
(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone;Methanone,(2-chloro-5-iodophenyl)(4-fluorophenyl)-;(2-Chloro-5-iodobenyl)(4-fluorophenyl)methanone;EmpagliflozinImpurity48;EnglenetImpurity16;2-chloro-4-fluoro-5-Iodobenzophenon;(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanon;2-Chloro-4'-fluoro-5-iodobenzophenone
Melting Point | 64-70℃ |
Boiling Point | 415℃ |
Density | 1.752 |
Flash Point | 205℃ |
Storage Condition | Under Inert Gas (Nitrogen or Argon) at 2–8 °c |
Solubility | Soluble in Chloroform (A Small Amount), Ethyl Acetate |
Form | Solid |
Color | Off White |
Empagliflozin Impurity 45 Is an Intermediate in the Synthesis of Empagliflozin. Empagliflozin Is a Sodium-Glucose Co-Transporter Type 2 Inhibitor Developed Jointly by Boehringer Ingelheim and Eli Lilly. Sglt-2 Inhibitors Are a New Type of Hypoglycemic Drug That Mainly Inhibits Sglt-2 Expressed in the Kidneys, Reduces Glucose Reabsorption by the Kidneys, And Increases Glucose Excretion in the Urine, Thereby Reducing Plasma Glucose Levels. Its Hypoglycemic Effect Is Independent of β-Cell Function and Insulin Resistance.