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2-Cyclohexen-1-one, 3-hydroxy-5-(2-methylphenyl)-, also known as 3-hydroxy-5-(o-tolyl)cyclohex-2-en-1-one, is a cyclic ketone with a molecular formula of C14H16O2. It features a hydroxyl group and a methylphenyl substituent on the cyclohexene ring, giving it unique structural and chemical properties.
Used in Perfume and Fragrance Industry:
2-Cyclohexen-1-one, 3-hydroxy-5-(2-methylphenyl)is used as a fragrance ingredient for its distinctive scent profile, contributing to the creation of various perfumes and fragrances.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Cyclohexen-1-one, 3-hydroxy-5-(2-methylphenyl)serves as a key intermediate compound for the production of pharmaceuticals and other fine chemicals, owing to its reactive functional groups and structural features.
Used in Research and Development:
Due to its unique properties, 2-Cyclohexen-1-one, 3-hydroxy-5-(2-methylphenyl)also holds potential in research and development, where it can be explored for new applications and further understanding of its chemical behavior.

239132-47-9

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239132-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 239132-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,9,1,3 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 239132-47:
(8*2)+(7*3)+(6*9)+(5*1)+(4*3)+(3*2)+(2*4)+(1*7)=129
129 % 10 = 9
So 239132-47-9 is a valid CAS Registry Number.

239132-47-9Relevant academic research and scientific papers

Construction of Multiple-Substituted Chiral Cyclohexanes through Hydrogenative Desymmetrization of 2,2,5-Trisubstituted 1,3-Cyclohexanediones

Yu, Chang-Bin,Song, Bo,Chen, Mu-Wang,Shen, Hong-Qiang,Zhou, Yong-Gui

supporting information, p. 9401 - 9404 (2019/11/28)

The construction of chiral multiple-substituted cyclohexanes motifs is a challenging topic in organic synthesis. By the combination of desymmetrization and remote stereocontrol, a ruthenium-catalyzed transfer hydrogenative desymmetrization of 2,2,5-trisubstituted 1,3-cyclohexanediones has been successfully developed for the construction of chiral multiple-substituted cyclohexanes with high enantioselectivity and diastereoselectivity. When an ester group was introduced to the two-position, a hydrogenative desymmetrization/transesterification cascade occurred, affording the bicyclic lactones bearing three stereocenters, including two discrete stereocenters and one quaternary stereogenic center, with high enantioselectivity. The products are the multiple-substituted chiral cyclohexanes bearing the hydroxyl and carbonyl functional groups, which provide a new opportunity for further precise elaboration.

PROCESS FOR THE PRODUCTION OF OPTICALLY ACTIVE CYCLIC ENAMINONE DERIVATIVES

-

, (2008/06/13)

A process for the production of optically active cyclic enaminone derivatives characterized by aminating one of the carbonyl groups of a cyclic 1,3-diketone derivative having a symmetry plane to obtain an optically isomeric mixture of chiral cyclic enamin

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