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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 configuration refers to the arrangement of the hydroxyl groups on the same side of the molecule, while the threo configuration describes the relative positions of the hydroxyl groups on the two cyclohexane rings. rac-cis-threo-cis-2,2'-Dihydroxydicyclohexylmethan is of interest in the field of organic chemistry, particularly in the study of chiral compounds and their potential applications in pharmaceuticals and materials science.

6556-80-5

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6556-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6556-80-5 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 6556-80:
(6*6)+(5*5)+(4*5)+(3*6)+(2*8)+(1*0)=115
115 % 10 = 5
So 6556-80-5 is a valid CAS Registry Number.

6556-80-5Relevant 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 (2007/10/03)

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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