4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE

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Products Intro: Product Name:4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE
CAS:320-43-4
Purity:99% Package:1KG;0.00;USD|25KG;0.00;USD
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Products Intro: Product Name:4-Chloro-2-(trifluoromethyl)benzaldehyde
CAS:320-43-4
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Products Intro: Product Name:4-Chloro-2-(trifluoromethyl)benzaldehyde
CAS:320-43-4
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-04133

4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE manufacturers

4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE Basic information
Product Name:4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE
Synonyms:4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE;2-TRIFLUOROMETHYL-4-CHLOROBENZALDEHYDE;2-(Trifluoromthyl)-4-Chlorobenzaldehyde;4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE, 97%+;Benzaldehyde, 4-chloro-2-(trifluoromethyl)-;4-Chloro-2-(trifluoromethyl)benzald;4-Chloro-2-fluoro-7-methoxyacetophenone
CAS:320-43-4
MF:C8H4ClF3O
MW:208.57
EINECS:
Product Categories:Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde
Mol File:320-43-4.mol
4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE Structure
4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE Chemical Properties
Boiling point 218.5±40.0 °C(Predicted)
density 1.423±0.06 g/cm3(Predicted)
refractive index 1.4960
storage temp. 2-8°C, stored under nitrogen
form liquid
color Clear, colourless
Sensitive Air Sensitive
CAS DataBase Reference320-43-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-36-43
Safety Statements 26-36/37
Hazard Note Irritant
HS Code 2913000090
MSDS Information
4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE Usage And Synthesis
Synthesis
4-Chloro-2-(trifluoromethyl)benzonitrile

320-41-2

4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE

320-43-4

The general procedure for the synthesis of 4-chloro-2-trifluoromethylbenzaldehyde using 2-trifluoromethyl-4-chlorobenzonitrile as a starting material was as follows: 2-trifluoromethyl-4-chlorobenzonitrile (appropriate amount) was added to a mixed solution of formic acid (96%, 15 mL) and water (3 mL). Nickel-aluminum alloy (1260 mg) was then added. The reaction mixture was heated and reacted at 100 °C overnight. Upon completion of the reaction, the reaction mixture was diluted with ethyl acetate and filtered through diatomaceous earth to remove solid impurities. The filtrate was sequentially extracted with 1N sodium hydroxide solution and saturated aqueous sodium chloride solution. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated to give 4-chloro-2-trifluoromethylbenzaldehyde (555 mg, 87% yield). The product was characterized by 1HNMR (400 MHz, MeOH-d4): δ 10.29 (m, 1H), 8.10 (d, 1H, J = 8.4 Hz), 7.91 (d, 1H, J = 1.6 Hz), 7.85 (dd, 1H, J = 8.4,1.6 Hz).

References[1] Patent: WO2006/44454, 2006, A1. Location in patent: Page/Page column 63
4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE Preparation Products And Raw materials
Raw materials4-Chloro-2-(trifluoromethyl)benzonitrile
Preparation Products4-CHLORO-2-(TRIFLUOROMETHYL)BENZYL BROMIDE
Tag:4-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE(320-43-4) Related Product Information
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