40394-02-3 Usage
Uses
Used in Organic Synthesis:
2,4,6-Cycloheptatrien-1-one, 2-(4-methoxyphenyl)is utilized as a versatile intermediate in organic synthesis for the creation of new compounds. Its unique aromatic and conjugated structure allows for a wide range of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,4,6-Cycloheptatrien-1-one, 2-(4-methoxyphenyl)serves as a key building block for the development of novel drug candidates. Its aromatic and conjugated structure, along with the methoxyphenyl group, can be leveraged to design and synthesize new pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Compound Development:
2,4,6-Cycloheptatrien-1-one, 2-(4-methoxyphenyl)is employed as a valuable component in the development of novel chemical compounds. Its specific properties, such as solubility and reactivity, conferred by the methoxyphenyl group, make it an attractive candidate for the creation of new compounds with potential applications in various fields, including materials science, agrochemicals, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 40394-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,9 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40394-02:
(7*4)+(6*0)+(5*3)+(4*9)+(3*4)+(2*0)+(1*2)=93
93 % 10 = 3
So 40394-02-3 is a valid CAS Registry Number.
40394-02-3Relevant academic research and scientific papers
SUBSTITUTED TROPOLONE DERIVATIVES AND METHODS OF USE
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Page/Page column 16, (2014/01/09)
The compositions and methods described herein relate generally to substituted tropolone derivatives, which, among other features, are useful as histone deacetylase (HDAC) inhibitors.
Regio- and diastereoselective stepwise [8 + 3]-cycloaddition reaction between tropone derivatives and donor-acceptor cyclopropanes
Rivero, Alexandra R.,Fernandez, Israel,Sierra, Miguel Angel
supporting information, p. 4928 - 4931 (2013/10/22)
A novel SnCl4-catalyzed [8 + 3]-cycloaddition reaction between tropone derivatives and donor-acceptor aminocyclopropanes is described. The process leads to the formation of amino-substituted tetrahydrocyclohepta[b] pyrans with complete regio- and diastereoselectivity. Density functional theory calculations suggest that the cycloaddition occurs stepwise through an aromatic zwitterionic intermediate.
Tropolones as lead-like natural products: The development of potent and selective histone deacetylase inhibitors
Ononye, Sophia N.,Vanheyst, Michael D.,Oblak, E. Zachary,Zhou, Wangda,Ammar, Mohamed,Anderson, Amy C.,Wright, Dennis L.
supporting information, p. 757 - 761 (2013/09/02)
Natural products have long been recognized as a rich source of potent therapeutics but further development is often limited by high structural complexity and high molecular weight. In contrast, at the core of the thujaplicins is a lead-like tropolone scaf
