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alpha,alpha,alpha-Trifluoro-o-toluoyl chloride

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alpha,alpha,alpha-Trifluoro-o-toluoyl chloride Basic information

Product Name:
alpha,alpha,alpha-Trifluoro-o-toluoyl chloride
Synonyms:
  • 4-(trifluoromethyl)-benzoylchlorid
  • Benzoyl chloride, 4-(trifluoromethyl)-
  • p-Toluoyl chloride, alpha,alpha,alpha-trifluoro-
  • p-Trifluoromethyl benzoic acid chloride
  • 4-(TRIFLUOROMETHYL)BENZOYL CHLORIDE
  • 4-(TRIFLUORMETHYL)-BENZOYL CHLORIDE
  • ALPHA,ALPHA,ALPHA-TRIFLUORO-P-TOLUOYL CHLORIDE
  • α,α,α-Trifluor-p-toluoylchlorid
CAS:
329-15-7
MF:
C8H4ClF3O
MW:
208.57
EINECS:
206-342-9
Product Categories:
  • Acid Halides
  • Building Blocks
  • Miscellaneous
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Trifluoromethylbenzene serise
  • Benzotrifluoride Series
  • bc0001
Mol File:
329-15-7.mol
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alpha,alpha,alpha-Trifluoro-o-toluoyl chloride Chemical Properties

Melting point:
-3°C
Boiling point:
188-190 °C(lit.)
Density 
1.404 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.476(lit.)
Flash point:
173 °F
storage temp. 
Inert atmosphere,2-8°C
form 
Liquid
Specific Gravity
1.404
color 
Clear colorless to yellow
Water Solubility 
decomposes
Sensitive 
Lachrymatory
BRN 
391282
CAS DataBase Reference
329-15-7(CAS DataBase Reference)
NIST Chemistry Reference
4-(Trifluoromethyl)benzoyl chloride(329-15-7)
EPA Substance Registry System
Benzoyl chloride, 4-(trifluoromethyl)- (329-15-7)
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Safety Information

Hazard Codes 
C
Risk Statements 
34-29
Safety Statements 
26-36/37/39-45-8
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
10-19-21
Hazard Note 
Corrosive/Lachrymatory
TSCA 
T
HazardClass 
8
PackingGroup 
II
HS Code 
29163900

MSDS

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alpha,alpha,alpha-Trifluoro-o-toluoyl chloride Usage And Synthesis

Chemical Properties

clear colourless to yellow liquid

Uses

4-(Trifluoromethyl)benzoyl chloride is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff.

General Description

4-(Trifluoromethyl)benzoyl chloride undergoes microwave-promoted Suzuki-type coupling reaction with phenylboronic acid to yield 4-(trifluoromethyl)benzophenone.

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