ChemicalBook--->CAS DataBase List--->24257-93-0

24257-93-0

24257-93-0 Structure

24257-93-0 Structure
IdentificationBack Directory
[Name]

2-ACETYLBENZALDEHYDE 95
[CAS]

24257-93-0
[Synonyms]

Benzaldehyde, o-acetyl-
Benzaldehyde, 2-acetyl-
Ortho-acetylbenzaldehyde
2-ACETYLBENZALDEHYDE 95
2-Acetylbenzaldehyde 95%
2-Acetylbenzaldehyde,2-Formylacetophenone
[Molecular Formula]

C9H8O2
[MDL Number]

MFCD05865162
[MOL File]

24257-93-0.mol
[Molecular Weight]

148.16
Chemical PropertiesBack Directory
[Melting point ]

39-43 °C (lit.)
[Boiling point ]

268.8±23.0 °C(Predicted)
[density ]

1.117±0.06 g/cm3(Predicted)
[Fp ]

>230 °F
[storage temp. ]

2-8°C, stored under nitrogen
[form ]

crystalline solid
[color ]

White/off-white
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

3
[HS Code ]

2914409000
Spectrum DetailBack Directory
[Spectrum Detail]

2-ACETYLBENZALDEHYDE 95(24257-93-0)1HNMR
2-ACETYLBENZALDEHYDE 95(24257-93-0)FT-IR
Hazard InformationBack Directory
[Synthesis]

2-ETHYNYLBENZALDEHYDE

38846-64-9

2-ACETYLBENZALDEHYDE  95

24257-93-0

General procedure for the synthesis of 2-acetylbenzaldehyde using 2-ethynylbenzaldehyde as starting material: the general method was as follows: first, AgBArF (97.1 mg, 0.1 mmol) was accurately weighed and placed in a long-necked glass reactor, followed by the addition of 2-ethynylbenzaldehyde (1 mmol). Next, 10 μL of ethyl acetate (EtOAc) was added and stirred for 5 min. After that, n-dodecane (1 mmol), an internal standard, and 3 mL of deionized water were added, and the reaction device was placed in an oil bath at 80 °C with continuous stirring and heated for 12 to 24 hours. Upon completion of the reaction, the reaction device was opened and 3 mL of ethyl acetate (EtOAc) was added to it and stirred for 5 minutes, after which the organic phase was separated and collected. The organic phase was passed through a short silica gel column to remove possible impurities and subsequently analyzed by GC-MS. Finally, the product was purified by silica gel column chromatography using a hexane/ethyl acetate (EtOAc) solvent mixture as eluent. The purified product was structurally characterized by 1H NMR and ESI-MS.

[References]

[1] Tetrahedron Letters, 2014, vol. 55, # 8, p. 1444 - 1447
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