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Bicyclo[2.2.1]heptan-2-one, 3-methyl-, endo-, also known as 3-methylbicyclo[2.2.1]heptan-2-one or camphor, is an organic compound with the chemical formula C10H16O. It is a white crystalline substance that is derived from the wood of the camphor tree, Cinnamomum camphora. Bicyclo[2.2.1]heptan-2-one, 3-methyl-, endo- is a bicyclic ketone, featuring a seven-membered ring with two carbon atoms forming a bridge between two other carbon atoms. The endo-isomer refers to the spatial arrangement of the methyl group, which is positioned on the same side of the molecule as the ketone group. Camphor has a strong, pungent odor and is used in various applications, including as a natural insect repellent, in traditional medicine, and as a fragrance in perfumes and incense.

4154-60-3

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4154-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4154-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4154-60:
(6*4)+(5*1)+(4*5)+(3*4)+(2*6)+(1*0)=73
73 % 10 = 3
So 4154-60-3 is a valid CAS Registry Number.

4154-60-3Relevant academic research and scientific papers

Thermochemical Studies of Carbonyl Reactions. 4. Enthalpies of Hydrolysis of Norbornyl Ketals

Wiberg, Kenneth B.,Cunningham, Wells C.

, p. 679 - 684 (1990)

The dimethyl ketals of norbornanone and of eight methyl-substituted norbornanones were prepared, and the enthalpies of hydrolysis were determined.The compounds were chosen to provide a variety of steric interactions between the methyl substituents and the ketal group, much of which would be relieved on going to the ketone.The enthalpies of reaction varied by over 4 kcal/mol.The experimental data were modeled by molecular mechanics (MM2), and although a good correlation was found for the less substituted compounds, the ketal of camphor fell off the slope = 1 correlation line.The free energy changes were determined, and were found not to be well correlated with the enthalpy changes.

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