ChemicalBook--->CAS DataBase List--->90381-07-0

90381-07-0

90381-07-0 Structure

90381-07-0 Structure
IdentificationBack Directory
[Name]

5-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE
[CAS]

90381-07-0
[Synonyms]

Benzaldehyde, 5-chloro-2-(trifluoromethyl)-
[Molecular Formula]

C8H4ClF3O
[MDL Number]

MFCD03412204
[MOL File]

90381-07-0.mol
[Molecular Weight]

208.57
Chemical PropertiesBack Directory
[Boiling point ]

82-86℃
[density ]

1.423±0.06 g/cm3(Predicted)
[refractive index ]

1.4880
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

liquid
[color ]

Clear, colourless
[Sensitive ]

Air Sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Risk Statements ]

22-36-43
[Safety Statements ]

26-36/37
[HS Code ]

2913000090
Spectrum DetailBack Directory
[Spectrum Detail]

5-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE(90381-07-0)1HNMR
5-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE(90381-07-0)FT-IR
Hazard InformationBack Directory
[Synthesis]

5-CHLORO-2-(TRIFLUOROMETHYL)BENZYL ALCOHOL

261763-21-7

5-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE

90381-07-0

General procedure for the synthesis of 5-chloro-2-trifluoromethylbenzaldehyde from (5-chloro-2-trifluoromethylphenyl)methanol: (5-chloro-2-trifluoromethylphenyl)methanol (347 mg, 1.66 mmol) was dissolved in dichloromethane (10 mL). Pyridinium chlorochromate (717 mg, 3.32 mmol) was added to the solution and the reaction mixture was stirred for 2 hours at room temperature. After the reaction was completed, the reaction solution was diluted with ether and stirring was continued for 1 hour. Subsequently, the reaction mixture was filtered to remove insoluble impurities and the filtrate was concentrated to remove solvent. Finally, the crude product was purified by silica gel column chromatography using a hexane solution of 10% ethyl acetate as eluent to afford 5-chloro-2-trifluoromethylbenzaldehyde as a colorless oil (285 mg, 82% yield).1H NMR (400 MHz, MeOH-d4) δ 10.33 (s, 1H), 7.90 (s, 1H), 7.69 (d, 1H, J = 8.4 Hz), 7.54 (d, 1H, J = 8.4 Hz).

[References]

[1] Patent: WO2006/44454, 2006, A1. Location in patent: Page/Page column 13-14
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