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2,4,5-TRIFLUOROBENZYL CHLORIDE

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2,4,5-TRIFLUOROBENZYL CHLORIDE Basic information

Product Name:
2,4,5-TRIFLUOROBENZYL CHLORIDE
Synonyms:
  • 2,4,5-TRIFLUOROBENZYL CHLORIDE
  • 2,4,5-TRIFLUOROBENZYL CHORIDE
  • Benzene, 1-(chloromethyl)-2,4,5-trifluoro- (9CI)
  • 1-(Chloromethyl)-2,4,5-trifluorobenzene, alpha-Chloro-2,4,5-trifluorotoluene
  • Sitagliptin Impurity 70
  • Benzene, 1-(chloromethyl)-2,4,5-trifluoro-
  • alpha-Chloro-2,4,5-trifluorotoluene
CAS:
243139-71-1
MF:
C7H4ClF3
MW:
180.55
Product Categories:
  • Fluorine series
  • HALOMETYL
  • Miscellaneous
Mol File:
243139-71-1.mol
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2,4,5-TRIFLUOROBENZYL CHLORIDE Chemical Properties

Boiling point:
175℃
Density 
1,689 g/cm3
refractive index 
1.5050
Flash point:
65°C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
clear liquid
color 
Colorless to Almost colorless
InChI
InChI=1S/C7H4ClF3/c8-3-4-1-6(10)7(11)2-5(4)9/h1-2H,3H2
InChIKey
JMXPOOVDUVHJRO-UHFFFAOYSA-N
SMILES
C1(CCl)=CC(F)=C(F)C=C1F
CAS DataBase Reference
243139-71-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xn
Risk Statements 
34-36/37/38-20/21/22
Safety Statements 
26-36/37/39-36
RIDADR 
3265
Hazard Note 
Corrosive
HazardClass 
8
PackingGroup 
II
HS Code 
2903998090

MSDS

  • Language:English Provider:ALFA
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2,4,5-TRIFLUOROBENZYL CHLORIDE Usage And Synthesis

Chemical Properties

Colorless to Almost colorless clear liquid.

Uses

2,4,5-Trifluorobenzyl chloride is an oral dipeptidyl peptidase-4 (DPP-4) inhibitor that decreases in glucagon to improve control of blood sugar used for the treatment of type 1 diabetes, 79% of the dose excreted in the urine.

Uses

2,4,5-Trifluorobenzyl chloride is a useful research chemical.

Synthesis

On the four-neck flask, install a stirrer, a thermometer, a chlorine gas pipe and a reflux condenser. The reflux condenser is connected to the HCl absorption system, and a light source is installed near the flask.Add 146.0g 2,4,5-trifluorotoluene and 3.0g azobisisobutyronitrile into the reaction flask, stir and heat, and when the temperature rises to 110°C, add dry chlorine gas, and Using GC tracking, after about 3h of chlorine gas, stop the halogenating agent chlorine gas, cool the reactant, wash it with water to neutrality, dry and distill under reduced pressure to obtain 2,4,5-trifluorobenzyl chloride.

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