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Rac-cis-threo-cis-2,2'-Dihydroxydicyclohexylmethan is a complex organic compound with the molecular formula C14H24O2. It is a derivative of dicyclohexylmethan, featuring two hydroxyl groups (-OH) attached to the carbon atoms at the 2nd position of each cyclohexane ring. The compound's structure is characterized by a racemic mixture, indicating that it consists of equal amounts of both R and S enantiomers. The cis-threo configuration refers to the arrangement of the hydroxyl groups and the cyclohexane rings, with the hydroxyl groups being on the same side of the molecule and the cyclohexane rings being adjacent to each other. rac-cis-threo-cis-2,2'-Dihydroxydicyclohexylmethan is of interest in the field of organic chemistry, particularly in the study of stereochemistry and the synthesis of complex molecules with specific spatial arrangements.

6556-82-7

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6556-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6556-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6556-82:
(6*6)+(5*5)+(4*5)+(3*6)+(2*8)+(1*2)=117
117 % 10 = 7
So 6556-82-7 is a valid CAS Registry Number.

6556-82-7Relevant academic research and scientific papers

Hydroacridines XVIII [1]. Synthesis and NMR spectroscopic investigation of (4aα,8aβ,9aα,10aβ)-tetradecahydroacridine and some of its derivatives

Potmischil, Francisc,Vierhapper, Friedrich W.,Kalchhauser, Hermann

, p. 515 - 522 (1998)

The reductive amination of (R*,R*)-2,2′-methylene-bis-cyclohexanone (1) with methylamine and potassium borohydride affords a mixture of (4aα,8aβ,9aα,10aβ)- and (4aα,8aα,9aβ,10aα)-tetradecahydro-10-methylacridine (2, 3) in a ratio of approximately 1.3:1 in 57% overall yield. By N-demethylation of 2, via the N-nitrosamine 4 the first synthesis of (4aα,8aβ,9aα,10aβ)-tetradecahydroacridine (5) could be performed. The relative configurations and conformations of compounds 2-5 as well as the barrier of conformational inversion of 5 (ΔG#300 = 55.5 ± 0.4 kJ · mol-1) were determined by NMR spectroscopy.

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