16235-53-3 Usage
Structure
Cycloheptatriene ring with a methoxyphenyl group attached at the 2-position
Aromaticity
Aromatic compound
Applications
Organic synthesis and pharmaceutical research
Reactivity
Can undergo oxidation, reduction, and substitution reactions
Versatility
Serves as a building block for the synthesis of complex organic compounds
Solubility
Methoxyphenyl group contributes to solubility in different solvents
Reactivity in reaction conditions
Methoxyphenyl group enhances reactivity under various conditions
Check Digit Verification of cas no
The CAS Registry Mumber 16235-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,3 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16235-53:
(7*1)+(6*6)+(5*2)+(4*3)+(3*5)+(2*5)+(1*3)=93
93 % 10 = 3
So 16235-53-3 is a valid CAS Registry Number.
16235-53-3Relevant academic research and scientific papers
An oxidative rearrangement of 6-phenylbicyclo[3.2.0]heptan-6-ol to 1,1′-biphenyl-carbaldehydes: A mechanistic study
Ceylan, Mustafa,Findik, Esra,Secen, Hasan
experimental part, p. 559 - 568 (2009/02/07)
Acid-catalyzed rearrangement of 6-phenylbicyclo[3.2.0]heptan-6-ol gave 1,1′-biphenyl and 1,1′-biphenyl-carbaldehydes in small amounts as well as the expected rearrangement products. A detailed study of the reaction mechanism revealed that the conversion occurs via an oxidative process through the consecutive formation of cycloheptadienes, cycloheptatrienes, and 1,1′-biphenyls. The acid-catalyzed rearrangement of 6-phenylbicyclo[3.2.0] hept-2-en-6-ols gave 1- and 2-phenylcycloheptatrienes directly, from which 1,1′-biphenyl and 1,1′-biphenyl-carbaldehydes were obtained by oxidation.
