(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone cas 915095-86-2

(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone cas 915095-86-2

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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

 
 

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-4'-fluoro-5-iodobenzophenone

(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone Properties

Melting Point64-70℃
Boiling Point415℃
Density1.752
Flash Point205℃
Storage ConditionUnder Inert Gas (Nitrogen or Argon) at 2–8 °c
SolubilitySoluble in Chloroform (A Small Amount), Ethyl Acetate
FormSolid
ColorOff White

Usage and Synthesis of (2-Chloro-5-iodophenyl)(4-fluorophenyl)ketone

Overview

(2-Chloro-5-Iodophenyl)(4-Fluorophenyl)methanone 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.

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