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(1S,4S)-1-isopropenyl-3,3-dideuterio-4-methylcyclohexane is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the 1 and 4 carbon atoms having the S configuration. The compound features a cyclohexane ring, which is a six-carbon ring structure, with a methyl group attached to the 4th carbon. Additionally, it has an isopropenyl group (a propene with an additional methyl group) attached to the 1st carbon and two deuterium atoms (isotopes of hydrogen with one neutron) replacing the hydrogen atoms on the 3rd carbon. (1S,4S)-1-isopropenyl-3,3-dideuterio-4-methylcyclohexane is of interest in organic chemistry and may have potential applications in various fields due to its unique properties and reactivity.

73687-69-1

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73687-69-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73687-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,8 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73687-69:
(7*7)+(6*3)+(5*6)+(4*8)+(3*7)+(2*6)+(1*9)=171
171 % 10 = 1
So 73687-69-1 is a valid CAS Registry Number.

73687-69-1Upstream product

73687-69-1Relevant academic research and scientific papers

Optical Rotatory Dispersion Studies. 130. Additivity of Deuterium Octant Contributions in Cyclohexanone

Edgar, Mark T.,Barth, Guenther,Djerassi, Carl

, p. 2680 - 2684 (2007/10/02)

A comparison between the circular dichroism spectra of (4S)-3,3-dideuterio-4-methylcyclohexanone (1), (3R,4R)-3-deuterio-4-tert-butylcyclohexanone (2) and (3S,4R)-3-deuterio-4-tert-butylcyclohexanone (3) leads to the conclusion that the octant contributions of deuterium in the β-equatorial and β-axial positions of the cyclohexanone ring are additive.From the temperature-dependent circular dichroism spectra of 1 an energy difference of -1.1 kcal/mol was obtained for the conformations with the 4-methyl substituent in the axial and equatorial position, respectively.

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