18073-24-0 Usage
Carbazole core structure
The central framework of the compound is a carbazole ring, which is a tricyclic aromatic system with a fused six-membered benzene ring and a five-membered nitrogen-containing ring.
Schiff base group
A nitrogen-containing group (-N=CH-) is present in the compound, which is a Schiff base. This group is responsible for the compound's ability to participate in various chemical reactions and contributes to its potential biological activity.
Ethanamine moiety
The compound also contains an ethanamine group (-NH2), which is attached to the Schiff base group. This functional group can form hydrogen bonds and coordinate with metal ions, further contributing to the compound's reactivity and potential applications.
Organic synthesis and medicinal chemistry applications
The compound is commonly used in these fields due to its potential biological activity and ability to participate in various chemical reactions, such as forming new bonds or acting as a precursor for other compounds.
Context-dependent properties and applications
The specific properties and applications of the compound may vary depending on the context in which it is used, such as in drug development (e.g., as a potential pharmaceutical agent) or materials science (e.g., as a component in the synthesis of new materials).
Check Digit Verification of cas no
The CAS Registry Mumber 18073-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,7 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18073-24:
(7*1)+(6*8)+(5*0)+(4*7)+(3*3)+(2*2)+(1*4)=100
100 % 10 = 0
So 18073-24-0 is a valid CAS Registry Number.
18073-24-0Relevant academic research and scientific papers
Simple method for preparing ellipticine or substituted ellipticine
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Paragraph 0050; 0051; 0055-0056, (2020/05/14)
The invention relates to a synthesis process for preparing ellipticine. Ellipticine is obtained through six steps of reaction and three steps of crystallization separation, the target product total yield is high, column chromatography separation is not needed for an intermediate product and the target product, and the method is particularly suitable for large-scale preparation.
