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4-(4-methoxyphenyl)-3-phenyl-1,2-dihydronaphthalene is a complex organic compound with the molecular formula C25H22O. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, with a dihydro prefix indicating the presence of two hydrogen atoms attached to the carbon atoms of the naphthalene ring. The compound features a 4-methoxyphenyl group, which is a phenyl ring with a methoxy (-OCH3) substituent at the para position, and a phenyl group attached to the 3-position of the naphthalene core. This molecule is characterized by its unique structure, which combines the properties of naphthalene with the additional functional groups, potentially influencing its chemical reactivity, physical properties, and applications in various fields such as pharmaceuticals, materials science, and organic synthesis.

145-55-1

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145-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145-55-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145-55:
(5*1)+(4*4)+(3*5)+(2*5)+(1*5)=51
51 % 10 = 1
So 145-55-1 is a valid CAS Registry Number.

145-55-1Relevant academic research and scientific papers

Copper-catalyzed carboarylation of alkynes via vinyl cations

Walkinshaw, Andrew J.,Xu, Wenshu,Suero, Marcos G.,Gaunt, Matthew J.

, p. 12532 - 12535 (2013/09/23)

Copper-catalyzed arylation of electron rich alkynes reveals stabilized trisubstituted vinyl cation equivalents that react with pendant arene nucleophiles to form all carbon tetrasubstituted alkenes. The new process streamlines the synthesis of important medicinally relevant molecules.

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