835-25-6 Usage
Chemical class
Phenylpropanoids Tropinone belongs to the class of organic compounds known as phenylpropanoids, which are derived from phenylalanine and have a propyl side chain.
Structure
Ketone derivative Tropinone is a ketone derivative, which means it contains a carbonyl group (C=O) bonded to two carbon atoms.
Substituents
Three methoxy groups Tropinone has three methoxy groups (-OCH3) attached to the phenyl ring, which gives it unique properties and chemical reactivity.
Pharmacological activities
Tropinone is known to have various pharmacological activities, making it a subject of interest for medicinal applications.
Medicinal applications
Tropinone has been studied for its potential use in the development of new drugs and therapies.
Building block
Tropinone is used as a building block for the synthesis of other organic compounds in the pharmaceutical and chemical industries.
Applications
Tropinone has important applications in the field of chemistry and medicinal research, making it a valuable compound for further study and development.
Synonyms
Tropinone is also known as 1-(2,4,6-Trimethoxyphenyl)propan-2-one, which highlights its chemical structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 835-25-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 835-25:
(5*8)+(4*3)+(3*5)+(2*2)+(1*5)=76
76 % 10 = 6
So 835-25-6 is a valid CAS Registry Number.
835-25-6Relevant academic research and scientific papers
Philicity of Acetonyl and Benzoyl Radicals: A Comparative Experimental and Computational Study
Verschueren, Rik H.,Schmauck, Julie,Perryman, Michael S.,Yue, Hui-Lan,Riegger, Julian,Schweitzer-Chaput, Bertrand,Breugst, Martin,Klussmann, Martin
supporting information, p. 9088 - 9097 (2019/06/24)
In this work, the reactivities of acetonyl and benzoyl radicals in aromatic substitution and addition reactions have been compared in an experimental and computational study. The results show that acetonyl is more electrophilic than benzoyl, which is rath
Evidence that the availability of an allylic hydrogen governs the regioselectivity of the Wacker oxidation
Gaunt,Yu,Spencer
, p. 1844 - 1845 (2007/10/03)
The allylic hydrogen is found to have a dramatic effect on the regioselectivity of the Wacker oxidation, leading to the postulation that an agostic hydrogen or enyl (σ + π) complex helps to stabilise the key intermediate.
