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(Rac)-2-tritylcyclohexanol is a complex organic compound with the molecular formula C27H25O. It is a racemate, meaning it consists of equal amounts of both R and S enantiomers. (rac)-2-tritylcyclohexanol features a cyclohexanol core, which is a cyclohexane ring with a hydroxyl group attached to one of the carbon atoms. The trityl group, a triphenylmethyl group, is attached to the cyclohexanol core, providing the molecule with its unique structure and properties. (Rac)-2-tritylcyclohexanol is primarily used as a chiral auxiliary in organic synthesis, helping to control the stereochemistry of reactions and facilitate the formation of specific enantiomers. Its unique structure and properties make it a valuable tool in the field of asymmetric synthesis and the development of chiral drugs.

20167-86-6

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20167-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20167-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20167-86:
(7*2)+(6*0)+(5*1)+(4*6)+(3*7)+(2*8)+(1*6)=86
86 % 10 = 6
So 20167-86-6 is a valid CAS Registry Number.

20167-86-6Downstream Products

20167-86-6Relevant academic research and scientific papers

Trans-2-tritylcyclohexanol as a chiral auxiliary in permanganate-mediated oxidative cyclization of 2-methylenehept-5-enoates: Application to the synthesis of trans-(+)-linalool oxide

Al Hazmi, Ali M.,Sheikh, Nadeem S.,Bataille, Carole J.R.,Al-Hadedi, Azzam A.M.,Watkin, Sam V.,Luker, Tim J.,Camp, Nicholas P.,Brown, Richard C.D.

supporting information, p. 5104 - 5107 (2015/01/08)

The permanganate-mediated oxidative cyclization of a series of 2-methylenehept-5-eneoates bearing different chiral auxiliaries was investigated, leading to the discovery of trans-2-tritylcyclohexanol (TTC) as a highly effective chiral controller for the f

Intramolecular bonding in β-silyl ketones?

Peddle

, p. 115 - 121 (2007/10/15)

A comparison of the infrared carbonyl group absorption of 2-(triphenylsilyl)cyclohexanone and of 2-(triphenylmethyl)cyclohexanone provided evidence of intramolecular interaction between the silicon atom and the carbonyl group. A similar interaction was fo

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