3-Methylcyclohexanone CAS:591-24-2
Name:3-Methylcyclohexanone CAS:591-24-2 MF:C7H12O MW:112.17 EINECS:209-710-7 Appearance:Clear colorless to very slightly yellow liquid COA:Provide Sample:Negotiable Synonyms: Cyclohexanone, 3-methyl-
Categories:
Material Chemistry
Other Material Chemicals
Email:sale06@alfachem.cn
Product introduction
| PRODUCT NAME | 3-Methylcyclohexanone |
| CAS NO | 591-24-2 |
| MP | -73 °C |
| BP | 169-170 °C (lit.) |
| DENSITY | 0.914 g/mL at 25 °C (lit.) |
| STORAGE | 2-8°C |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of 3-Methylcyclohexanone CAS:591-24-2
3-Methylcyclohexanone CAS:591-24-2 is a molecule with an intramolecular hydrogen bond. The carbonyl group of this molecule can be found in the form of a ketone or an ester, which are both forms of organic compounds that contain a carbonyl group.
3-Methylcyclohexanone has been synthesized from cyclohexane and acetaldehyde by dehydration.It is soluble in water, ethanol, ether, chloroform, and benzene but not in benzene sulfonic acid or nitrobenzene. 3-Methylcyclohexanone has been used as an intermediate for other chemical reactions such as the synthesis of dyes and pharmaceuticals.

Applications of 3-Methylcyclohexanone CAS:591-24-2
1)Enhanced Enantioselectivity
3-Methylcyclohexanone has been studied for its enhanced enantioselectivity in crystallization processes.
2)Conformational Analysis
The compound's conformational analysis has been a subject of interest.
3)Molecular Dynamics Simulation
3-Methylcyclohexanone has been used in computer simulations to understand rotation/translation coupling in its enantiomer and racemic mixtures.
4)Catalysis and Reaction Mechanism
5)Vibrational Raman Optical Activity
6)Molecular Structures and NMR Spectroscopy
7)Dipole Moment Measurement
The measurement of the dipole moment of 3-Methylcyclohexanone in the gas phase has been achieved through the study of its rotational spectrum, providing improved spectroscopic constants
8)Stereochemical Aspects in Metabolism
3-Methylcyclohexanone has been studied for its stereochemical aspects in metabolism, especially in terms of the transformation of its isomeric forms in biological systems
9)Enantiospecific Adsorption
The enantiospecific adsorption of 3-Methylcyclohexanone on naturally chiral surfaces has been demonstrated, providing insights into the interactions between chiral molecules and surfaces
10)Clathrate Hydrate Formation
Studies have also explored the formation of clathrate hydrates in systems containing 3-Methylcyclohexanone, revealing new data on the equilibrium pressure and temperature conditions in these systems
Key words:
Related Products
Related Products
Inquiry