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(1RS,2SR,4SR)-p-menthane-1,2-diol, also known as (1R,2S,4S)-p-menthane-1,2-diol, is a chiral organic compound with the molecular formula C10H20O2. It is a diastereomer of the more common (1R,2S,4R)-p-menthane-1,2-diol, which is a component of the essential oil of peppermint. (1RS,2SR,4SR)-p-menthane-1,2-diol is characterized by its unique arrangement of hydroxyl groups at the 1, 2, and 4 positions of the p-menthane ring system. It is a colorless liquid with a distinct odor and is used in the synthesis of various pharmaceuticals and fragrances. Due to its chiral nature, it exhibits different physical and chemical properties compared to its enantiomers and diastereomers, making it an important compound in the field of stereochemistry and asymmetric synthesis.

59168-67-1

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59168-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59168-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,6 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59168-67:
(7*5)+(6*9)+(5*1)+(4*6)+(3*8)+(2*6)+(1*7)=161
161 % 10 = 1
So 59168-67-1 is a valid CAS Registry Number.

59168-67-1Relevant academic research and scientific papers

Eco-friendly kinetic separation of trans-limonene and carvomenthene oxides

Santosh Kumar, S Chandrappa,Manjunatha, Javagal Rangaswamy,Srinivas, Pullabhatla,Bettadaiah, Bheemanakere Kemapaiah

, p. 875 - 880 (2014/07/07)

Kinetic separation of trans-limonene oxide and trans-carvomenthene oxide was achieved in high yield by selective ring opening of their cis-epoxides in the presence of InCl3 catalyst in water. Catalytic activity of InCl3 was conserved

Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes

Santi, Claudio,Di Lorenzo, Rosalia,Tidei, Caterina,Bagnoli, Luana,Wirth, Thomas

, p. 10530 - 10535,6 (2012/12/12)

The selenium atom of the selenocysteine plays a crucial role in the reduction of peroxides. Herein we showed that, in the absence of a thiol cofactor, the same aminoacid efficiently catalyzed the dihydroxylation of carbon-carbon double bonds leading to the stereoselective formation of 1,2-diols at room temperature and in on water conditions. Alternatively, in the presence of methanol, the corresponding β-methoxyalcohol can be prepared. The stereoselectivity of the reaction will be discussed and NMR evidences of the actual catalyst are here reported.

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