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(5S)-(-)-5β-(1-Hydroxy-1-methylethyl)-1-methyl-1,3-cyclohexadien is a complex organic compound characterized by its unique molecular structure. It is a chiral molecule, indicated by the "5S" notation, which specifies the spatial arrangement of its atoms. The compound features a cyclohexadien ring, which is a six-carbon ring with alternating double bonds, and a hydroxyl group (-OH) attached to a methyl group (-CH3) on the 1-position. Additionally, it has a methyl group on the 5-position of the ring, which is in the β-configuration. (5S)-(-)-5β-(1-Hydroxy-1-methylethyl)-1-methyl-1,3-cyclohexadien is a stereoisomer, meaning it has the same molecular formula as other isomers but differs in the arrangement of atoms in space, leading to distinct physical and chemical properties.

5208-31-1

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5208-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5208-31-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5208-31:
(6*5)+(5*2)+(4*0)+(3*8)+(2*3)+(1*1)=71
71 % 10 = 1
So 5208-31-1 is a valid CAS Registry Number.

5208-31-1Relevant academic research and scientific papers

Formation of 1,2-Dioxolanes from Cyclopropanes

Ruecker, Gerhard,Frey, Klaus

, p. 389 - 392 (2007/10/02)

The already known carenols 5 and 7 are obtained by stereoselective oxirane cleavage of (1S,3S,4R,6R)-(+)-3α,4α-epoxycarane (4).Autoxidation of the ketone 8, derived from 7, failed to give any 1,2-dioxolane derivatives. 5 is converted to the hydroperoxide

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