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Thermo Scientific Chemicals
2-Ethylcyclohexanone, 99%
CAS: 4423-94-3 | C8H14O | 126.199 g/mol
化学物質識別子
CAS4423-94-3
IUPAC Name2-ethylcyclohexan-1-one
Molecular FormulaC8H14O
InChI KeyWKYYYUWKFPFVEY-UHFFFAOYNA-N
SMILESCCC1CCCCC1=O
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥98.5%
Refractive Index1.4500-1.4530 @ 20°C
2-Ethylcyclohexanone is used as a pharmaceutical intermediate. 2-Methyl and 2-ethyl derivatives of cyclohexanone were allowed to react with deuterium in tBuOD using platinum group metals as catalysts to study the substituent effects in heterogeneous catalysis.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Ethylcyclohexanone is used as a pharmaceutical intermediate. 2-Methyl and 2-ethyl derivatives of cyclohexanone were allowed to react with deuterium in tBuOD using platinum group metals as catalysts to study the substituent effects in heterogeneous catalysis.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Store at room temperature. Incompatible with strong oxidizing agents.
2-Ethylcyclohexanone is used as a pharmaceutical intermediate. 2-Methyl and 2-ethyl derivatives of cyclohexanone were allowed to react with deuterium in tBuOD using platinum group metals as catalysts to study the substituent effects in heterogeneous catalysis.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Store at room temperature. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Shousuke Teratani, Kazunori Tanaka.; Haruo Ogawa.; Kazuo Taya. Substituent effects in heterogeneous catalysis: VIII. Reactions of 2-methyl- and 2-ethylcyclohexanone with deuterium catalyzed by platinum metals. J. Catal. 1981, 70 (2),347-355 .
- Herbert C. Brown.; Milorad M. Rogic.; Michael W. Rathke. Reaction of organoboranes with .alpha.-bromo ketones under the influence of potassium tert-butoxide in tetrahydrofuran. A new technique for the .alpha.-alkylation of ketones.J. Am. Chem. Soc. 1968, 90 (22),6218-6219 .