ChemicalBook--->CAS DataBase List--->23790-39-8

23790-39-8

23790-39-8 Structure

23790-39-8 Structure
IdentificationBack Directory
[Name]

2,6-Di-tert-butyl-4-Methylcyclohexanone (Mixture of isoMers)
[CAS]

23790-39-8
[Synonyms]

2,6-Di-tert-butyl-4-methylcyclohexanone
2,6-ditert-butyl-4-methylcyclohexan-1-one
Cyclohexanone,2,6-bis(1,1-dimethylethyl)-4-methyl-
2,6-Di-tert-butyl-4-Methylcyclohexanone (Mixture of isoMers)
2,6-Di-tert-butyl-4-methylcyclohexanone(mixtureofisomers)>
2,6-Di-tert-butyl-4-methylcyclohexanone (mixture of isomers)
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C15H28O
[MDL Number]

MFCD27976821
[MOL File]

23790-39-8.mol
[Molecular Weight]

224.38
Chemical PropertiesBack Directory
[Boiling point ]

134°C/20mmHg(lit.)
[density ]

0.878±0.06 g/cm3(Predicted)
[refractive index ]

1.4590-1.4630
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Almost colorless
[CAS DataBase Reference]

23790-39-8
Questions And AnswerBack Directory
[Uses]

2,6-Di-tert-butyl-4-methylcyclohexanone can be used as a synthetic intermediate for the preparation of 2,6-di-tert-butyl-4-methylcyclohexanol. Using di-tert-butyl-4-methylphenol and isopropanol as starting materials, the reaction is carried out in a Raney nickel catalyst and a high-pressure reactor to first obtain 2,6-di-tert-butyl-4-methylcyclohexanone. Then, the cyclohexanone is reduced with lithium aluminum hydride to obtain the cyclohexanol product. 2,6-Di-tert-butyl-4-methylcyclohexanol is mainly used in photography, printing and dyeing, and as a medical intermediate.
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

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

2914.29.5000
Hazard InformationBack Directory
[Synthesis]

2,6-Di-tert-butyl-4-methylcyclohexanone was obtained by adding 10-15% Raney nickel catalyst (mass ratio) and a certain amount of di-tert-butyl-4-methylphenol to an autoclave and reacting at 160°C to 250°C, reaction time 1h to 2h and reaction pressure 10-1
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