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4-Fluoro-2-(trifluoromethyl)benzaldehyde

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4-Fluoro-2-(trifluoromethyl)benzaldehyde Basic information

Product Name:
4-Fluoro-2-(trifluoromethyl)benzaldehyde
Synonyms:
  • 2-TRIFLUOROMETHYL-4-FLUOROBENZALDEHYDE
  • 2-Trifluoromethoxy-4-Fluorobenzaldehyde 4-Fluoro-2-(Trifluoromethyl) Benzaldehyde
  • 2-Trifluoromethoxy-4-Fluorobenzaldehyde
  • 4-Fluoro-2-(trilfuoromethyl)benzaldehyde
  • alpha,alpha,alpha,4-Tetrafluoro-o-tolualdehyde
  • 4-Fluoro-2-(Trifluoromethyl)be
  • à,à,à,4-tetrafluoro-o-tolualdehyde
  • 4-Fluoro-2-(trifluoromethyl)benzaldehyde 97%
CAS:
90176-80-0
MF:
C8H4F4O
MW:
192.11
Product Categories:
  • Fluorine series
  • Benzaldehyde
  • Aldehydes
  • C8
  • Carbonyl Compounds
  • Aromatic Aldehydes & Derivatives (substituted)
Mol File:
90176-80-0.mol
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4-Fluoro-2-(trifluoromethyl)benzaldehyde Chemical Properties

Boiling point:
114 °C (lit.)
Density 
1.408 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.452(lit.)
Flash point:
134 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
clear liquid
color 
Colorless to Light yellow to Light orange
Sensitive 
Air Sensitive
BRN 
5932091
InChI
1S/C8H4F4O/c9-6-2-1-5(4-13)7(3-6)8(10,11)12/h1-4H
InChIKey
NONOHEMDNFTKCZ-UHFFFAOYSA-N
SMILES
Fc1ccc(C=O)c(c1)C(F)(F)F
CAS DataBase Reference
90176-80-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
RIDADR 
UN 1989 3/PG 3
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
3
PackingGroup 
III
HS Code 
29130000
Storage Class
3 - Flammable liquids
Hazard Classifications
Eye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3

MSDS

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4-Fluoro-2-(trifluoromethyl)benzaldehyde Usage And Synthesis

Chemical Properties

clear colorless liquid

Uses

Starting material for Fevipiprant. 4-Fluoro-2-(trifluoromethyl)benzaldehyde is also a reagent in the preparation of numerous inhibitors against proteins such as CRTH2, DP2 Receptor and Hepatitis B Virus (HBV) Capsid.

General Description

4-Fluoro-2-(trifluoromethyl)benzaldehyde is an organic fluorinated building block. It participates in the synthesis of diphenylthioethers. It also participates in the preparation of 1-cyano derivative of nilutamide.

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