ChemicalBook--->CAS DataBase List--->96184-81-5

96184-81-5

96184-81-5 Structure

96184-81-5 Structure
IdentificationMore
[Name]

4-OXO-CYCLOHEXANECARBOXALDEHYDE
[CAS]

96184-81-5
[Synonyms]

4-OXO-CYCLOHEXANECARBOXALDEHYDE
4-OXO-CYCLOHEXANECARBOXYALDEHYDE
Cyclohexanecarboxaldehyde, 4-oxo-(9CI)
Cyclohexanone-4-carboxaldehyde
4-Formylcyclohexanone
[EINECS(EC#)]

200-589-5
[Molecular Formula]

C7H10O2
[MDL Number]

MFCD04972553
[Molecular Weight]

126.15
[MOL File]

96184-81-5.mol
Chemical PropertiesBack Directory
[Boiling point ]

223 ºC
[density ]

1.151
[Fp ]

81 ºC
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[Appearance]

Colorless to light yellow Liquid
[CAS DataBase Reference]

96184-81-5(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[HS Code ]

2914409000
Spectrum DetailBack Directory
[Spectrum Detail]

4-OXO-CYCLOHEXANECARBOXALDEHYDE(96184-81-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,4-Dioxaspiro[4.5]decane, 8-(methoxymethylene)-

96184-80-4

4-OXO-CYCLOHEXANECARBOXALDEHYDE

96184-81-5

Step 2: Synthesis of 4-oxocyclohexanecarboxaldehyde; 8-(methoxymethylene)-1,4-dioxaspiro[4.5]decane (30 g, 0.16 mol) was dissolved in 1,4-dioxane (60 mL), H2O (30 mL) was added and concentrated. To this solution, HCl solution (120 mL, 1.4 mol) was slowly added at room temperature. The reaction mixture was stirred for 1 hour at room temperature. Upon completion of the reaction, liquid-liquid partition extraction was performed with ethyl acetate (150 mL) and H2O (150 mL). The organic layer was separated, dried with anhydrous Na2SO4 and concentrated under reduced pressure to give the crude product 4-oxocyclohexanecarboxaldehyde (15.3 g, 86.9% yield) as a colorless oil. The crude product was directly used in the next reaction without further purification.1H NMR (400 MHz, CDCl3) δ 9.71 (s, 1H), 2.64-2.62 (m, 1H), 2.41-2.29 (m, 5H), 2.20-2.15 (m, 2H), 1.94-1.89 (m, 2H).

[References]

[1] Patent: WO2008/94574, 2008, A2. Location in patent: Page/Page column 50
[2] Molecular Crystals and Liquid Crystals (1969-1991), 1985, vol. 131, p. 327 - 342
[3] Patent: US5238602, 1993, A
[4] Patent: US4565425, 1986, A
[5] Patent: US4915480, 1990, A
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