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1-p-Tolyl-cycloheptanol is a chemical compound with the molecular formula C14H18O. It is a derivative of cycloheptanol, featuring a p-tolyl group (a methyl group attached to a phenyl ring) at the 1-position. This organic compound is characterized by its unique structure, which combines a seven-membered cyclic alcohol with an aromatic substituent. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties. The compound is typically synthesized through various methods, including cyclization reactions and reduction processes. Its applications span across different industries, making it a valuable component in the development of new chemical entities.

77826-31-4

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77826-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77826-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,2 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77826-31:
(7*7)+(6*7)+(5*8)+(4*2)+(3*6)+(2*3)+(1*1)=164
164 % 10 = 4
So 77826-31-4 is a valid CAS Registry Number.

77826-31-4Relevant academic research and scientific papers

Iodobenzene-catalyzed oxidative cleavage of olefins to carbonyl compounds

Du, Lele,Wang, Zechao,Wu, Junliang

supporting information, (2020/07/20)

A metal-free approach for the oxidative cleavage of carbon–carbon double bonds of olefins to carbonyl compounds was established by using oxidant m-CPBA and non-metallic organocatalyst PhI in toluene/H2O. A broad scope of aromatic olefins was used. All the reactions proceeded smoothly at 35 °C in short reaction time to furnish the respective mono- and double carbonyl compounds selectively in moderate to good yields.

Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes

Lee, Gon-Ann,Lee, Hsin-Yi,Wang, Wen-Chieh,Cherng, Chih-Hwa

, p. 2956 - 2961 (2014/04/17)

Auto de-bromine-coupling reactions of 1-aryl-7-bromocycloheptenes to a new series of [7-6-6] tricyclic system were described. A variety of substituents at the para-position of the phenyl were amenable to this transformation, including electron-donating groups and halides. The presence of electron-donating groups resulted in a more efficient reaction, with higher yields than the case of halides.

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