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(1S,4R)-(+)-2,2-Dimethyl-4-tert-butylcyclohexan-1-ol is a chiral, cyclic alcohol with a molecular formula of C12H24O. It features a cyclohexane ring with two methyl groups at the 2-position, a tert-butyl group at the 4-position, and a hydroxyl group at the 1-position. (1S,4R)-(+)-2,2-Dimethyl-4-tert-butylcyclohexan-1-ol is known for its unique stereochemistry, with the 1S and 4R configurations indicating the specific arrangement of substituents on the chiral centers. It is often used in organic synthesis, particularly in the preparation of complex molecules that require precise stereocontrol. The compound's physical properties, such as its boiling point and solubility, can be influenced by its stereochemistry and the presence of the bulky tert-butyl group.

73395-39-8

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73395-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73395-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,9 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73395-39:
(7*7)+(6*3)+(5*3)+(4*9)+(3*5)+(2*3)+(1*9)=148
148 % 10 = 8
So 73395-39-8 is a valid CAS Registry Number.

73395-39-8Relevant academic research and scientific papers

Synthesis of Chiral Conformationally Fixed Cyclohexanones

Konopelski, Joseph P.,Djerassi, Carl

, p. 2297 - 2301 (2007/10/02)

Two syntheses of (R)-(+)-2,2-dimethyl-4-tert-butylcyclohexanone (1) are presented.Related 4-alkylcyclohexanones (intermediates in the syntheses) bear other (potential) conformational anchoring groups.The key steps in the syntheses are the opening of the cyclobutane ring of (+)-3,3-dimethylnopinone (10) by either pyrolysis or reaction with BBr3.The high optical purity of the final compound was determined by analysis of the 19F NMR spectrum of the diastereomeric ester mixture obtained from the reaction of alcohol (+)-14b with (S)-(+)-MTPA chloride

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