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2-(4-fluoronaphthalen-1-yl)cyclohexan-1-one is a complex organic compound characterized by its unique molecular structure. It features a cyclohexanone ring, which is a six-membered carbon ring with a ketone group (C=O) attached to the second carbon. The naphthalene moiety, a fused pair of benzene rings, is substituted with a fluorine atom at the 4-position, and this naphthalenyl group is attached to the cyclohexanone ring. 2-(4-fluoronaphthalen-1-yl)cyclohexan-1-one is likely to have specific chemical properties due to the presence of the fluorine atom, which can influence reactivity and physical properties. It may be used in the synthesis of various pharmaceuticals, agrochemicals, or as an intermediate in organic chemistry. The exact applications and properties would depend on the specific context in which 2-(4-fluoronaphthalen-1-yl)cyclohexan-1-one is being considered.

1827-58-3

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1827-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1827-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1827-58:
(6*1)+(5*8)+(4*2)+(3*7)+(2*5)+(1*8)=93
93 % 10 = 3
So 1827-58-3 is a valid CAS Registry Number.

1827-58-3Relevant academic research and scientific papers

Palladium-catalyzed asymmetric hydrogenation of 2-aryl cyclic ketones for the synthesis oftranscycloalkanols through dynamic kinetic resolution under acidic conditions

Li, Xiang,Zhao, Zi-Biao,Chen, Mu-Wang,Wu, Bo,Wang, Han,Yu, Chang-Bin,Zhou, Yong-Gui

, p. 5815 - 5818 (2020)

The first efficient palladium-catalyzed asymmetric hydrogenation of 2-aryl cyclic ketones has been described through dynamic kinetic resolution under acidic conditions, providing a facile access to chiraltranscycloalkanol derivatives with excellent enantioselectivities.

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