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(2R,3R)-2,3-dicyclohexylbutane-1,4-diol is a chiral organic compound characterized by its unique molecular structure, consisting of two cyclohexyl groups attached to a butane-1,4-diol backbone. (2R,3R)-2,3-dicyclohexylbutane-1,4-diol is a specific stereoisomer, with the R configuration at both the 2nd and 3rd carbon atoms, which significantly influences its physical and chemical properties. It is an important intermediate in the synthesis of various pharmaceuticals and specialty chemicals, owing to its ability to form complex molecular architectures. The compound's chirality and rigid cyclic structure make it a valuable building block in the development of enantiomerically pure compounds, which are crucial in many biological and medicinal applications.

64029-69-2

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64029-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64029-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,2 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64029-69:
(7*6)+(6*4)+(5*0)+(4*2)+(3*9)+(2*6)+(1*9)=122
122 % 10 = 2
So 64029-69-2 is a valid CAS Registry Number.

64029-69-2Downstream Products

64029-69-2Relevant academic research and scientific papers

Influence of β-arranged substituents in chiral seven-membered rhodium diphosphine rings on asymmetric hydrogenation of amino acid precursors

Krause, Hanswalter,Sailer, Cornelia

, p. 271 - 279 (2007/10/02)

Investigations concerning the optical induction in asymmetric hydrogenation reactions confirm the stereochemical control function of mono- and di-substituents in seven-membered chelate ring diphosphines, whereby the bulkiness of substituents in the backbone of the ligands is reflected in higher enantioselectivities.

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