1546-11-8 Usage
Explanation
The compound consists of 12 carbon atoms, 13 hydrogen atoms, and 1 fluorine atom.
Explanation
The core structure is a benzene ring with a fluorine atom attached to the fourth carbon. A cyclohexene group is connected to the first carbon of the benzene ring.
Explanation
It is an aromatic compound containing a fluorine atom, which is part of the benzene ring.
Explanation
The compound has a liquid state under normal environmental conditions, with no color.
Explanation
It serves as a starting material or intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical industry.
Explanation
The compound is used to produce different organic compounds through various chemical reactions.
Explanation
The specific arrangement of atoms in the molecule makes it useful for creating novel pharmaceuticals and other materials with potential applications.
Molecular structure
Benzene ring substituted with a fluorine atom at the 4th position and a cyclohexene group at the 1st position.
Type of compound
Fluoroaromatic compound
Physical state
Clear, colorless liquid at room temperature
Usage
Building block in organic synthesis and pharmaceutical research
Application
Reagent in chemical reactions
Unique molecular structure
Valuable tool in the development of new drugs and materials
Check Digit Verification of cas no
The CAS Registry Mumber 1546-11-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1546-11:
(6*1)+(5*5)+(4*4)+(3*6)+(2*1)+(1*1)=68
68 % 10 = 8
So 1546-11-8 is a valid CAS Registry Number.
1546-11-8Relevant articles and documents
Photocatalyzed Transition-Metal-Free Oxidative Cross-Coupling Reactions of Tetraorganoborates**
Music, Arif,Baumann, Andreas N.,Boser, Florian,Müller, Nicolas,Matz, Florian,Jagau, Thomas C.,Didier, Dorian
supporting information, p. 4322 - 4326 (2021/02/11)
Readily accessible tetraorganoborate salts undergo selective coupling reactions under blue light irradiation in the presence of catalytic amounts of transition-metal-free acridinium photocatalysts to furnish unsymmetrical biaryls, heterobiaryls and arylated olefins. This represents an interesting conceptual approach to forge C?C bonds between aryl, heteroaryl and alkenyl groups under smooth photochemical conditions. Computational studies were conducted to investigate the mechanism of the transformation.
Catalytic hydrogen atom transfer (HAT) for sustainable and diastereoselective radical reduction
Gansaeuer, Andreas,Klatte, Max,Braendle, Gerhard M.,Friedrich, Joachim
, p. 8891 - 8894 (2012/10/08)
Going cyclic! A catalytic cycle and cyclic transition states enable a novel sustainable and catalytic hydrogen atom transfer (HAT) for highly diastereoselective radical reductions. Readily available nontoxic silanes are the terminal reductants for epoxides that are opened by bifunctional titanocene(III) hydride catalysts. Copyright
Nickel-catalyzed cross-couplings of cyclohexenyl phosphate and arylboronic acids
Nan, Yang,Yang, Zhen
, p. 3321 - 3324 (2007/10/03)
The Nickel-catalyzed cross-coupling reaction of cyclohexenylphosphate with a variety of arylboronic acids is described here for the first time. This methodology opens the door to other palladium or nickel-catalyzed coupling reactions involving vinyl phosphates.
