ChemicalBook--->CAS DataBase List--->403-32-7

403-32-7

403-32-7 Structure

403-32-7 Structure
IdentificationBack Directory
[Name]

(4-FLUORO-PHENYL)-OXO-ACETALDEHYDE
[CAS]

403-32-7
[Synonyms]

NSC 402742
4-FLUOROPHENYLGLYOXAL
(p-Fluorophenyl)glyoxal
(4-FLUORO-PHENYL)-OXO-ACETALDEHYDE
4-Fluoro-α-oxo-benzeneacetaldehyde
Benzeneacetaldehyde, 4-fluoro-α-oxo-
4-fluoro-alpha-oxo-benzeneacetaldehyd
4-fluoro-alpha-oxobenzeneacetaldehyde
Benzeneacetaldehyde, 4-fluoro-.alpha.-oxo-
[Molecular Formula]

C8H5FO2.H2O
[MDL Number]

MFCD01733156
[MOL File]

403-32-7.mol
[Molecular Weight]

170.14
Chemical PropertiesBack Directory
[Melting point ]

84-88℃
[Boiling point ]

115℃/35mm
[density ]

1.241±0.06 g/cm3(Predicted)
[RTECS ]

CY1440000
[solubility ]

Chloroform, Methanol
[form ]

Solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

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

36/37/38
[Safety Statements ]

26-36/37/39
[Toxicity]

mouse,LD50,intraperitoneal,681mg/kg (681mg/kg),BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION,Journal of the Indian Chemical Society. Vol. 60, Pg. 369, 1983.
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

4-Fluoro-α-oxo-benzeneacetaldehyde (cas# 403-32-7) is a compound useful in organic synthesis.
[Synthesis]

4-Fluoroacetophenone

403-42-9

(4-FLUORO-PHENYL)-OXO-ACETALDEHYDE

403-32-7

The general procedure for the synthesis of 4-fluorobenzoylformaldehyde from 4-fluoroacetophenone was as follows: selenium dioxide (6.70 g, 61.0 mmol) was added to a mixed solution of dioxane (100 mL) and water (3 mL) containing 4-fluoroacetophenone (8.43 g, 61.0 mmol). The resulting mixture was heated at 55 °C until selenium dioxide was completely dissolved. Subsequently, the reaction mixture was refluxed for 5 to 6 hours. After monitoring the completion of the reaction by thin layer chromatography (TLC), the mixture was filtered and the filtrate was concentrated under vacuum to obtain a viscous oily substance. Water (50 mL) was added to the oily substance and the resulting mixture was stirred for 12 hours. Afterwards, the solid formed was collected on a filter, washed with water (25 mL) and dried under vacuum to finally obtain 4-fluorophenylglyoxal (6.60 g, 85% yield).1H NMR (400 MHz, CDCl3) δ: 7.18 (m, 2H), 8.11 (d, 2H), no signal for aldehyde CHO was observed.

[References]

[1] Patent: WO2011/95625, 2011, A1. Location in patent: Page/Page column 94
[2] Tetrahedron Letters, 2017, vol. 58, # 7, p. 658 - 662
[3] Patent: WO2007/39821, 2007, A2. Location in patent: Page/Page column 16
[4] Journal of Heterocyclic Chemistry, 1981, vol. 18, p. 1651 - 1653
[5] Angewandte Chemie - International Edition, 2016, vol. 55, # 36, p. 10890 - 10894
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