86456-50-0 Usage
Explanation
The compound consists of 20 carbon atoms, 19 hydrogen atoms, 1 nitrogen atom, and 1 oxygen atom.
Explanation
The compound has a cyclopropane ring structure with an amide functional group attached to it.
Explanation
The cyclopropane ring has a methyl group (CH3) and two phenyl groups (C6H5) attached to it, which contribute to its chemical structure and properties.
Explanation
1-Methyl-2,2-diphenylcyclopropanecarboxamide is used as a starting material or intermediate in the synthesis of various biologically active products.
Explanation
The compound serves as a building block for the development of new drugs and other biologically active molecules.
Explanation
Research has been conducted on the compound's potential to be used as a treatment for conditions such as seizures and epilepsy.
Explanation
The compound has been studied for its potential applications in the creation of new drugs and therapeutic agents.
Chemical class
Cyclopropanecarboxamide derivative
Substituents
Methyl group and two phenyl groups
Usage in organic synthesis
Building block
Medicinal chemistry applications
Synthesis of pharmaceuticals and biologically active compounds
Pharmacological properties
Potential anticonvulsant and antiepileptic agent
Investigation for potential use
Development of new pharmaceuticals
Check Digit Verification of cas no
The CAS Registry Mumber 86456-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86456-50:
(7*8)+(6*6)+(5*4)+(4*5)+(3*6)+(2*5)+(1*0)=160
160 % 10 = 0
So 86456-50-0 is a valid CAS Registry Number.
86456-50-0Relevant academic research and scientific papers
Electrochemical Oxidation of Benzophenone Hydrazones
Chiba, Toshiro,Okimoto, Mitsuhiro,Nagai, Hiroshi,Takata, Yoshiyuki
, p. 2968 - 2972 (2007/10/02)
The anodic oxidation of benzophenone hydrazones (1) was found to give several products, depending upon the electrolysis conditions employed such as electrode material, temperature, and electrolyte composition.For example, the oxidation using a platinum anode at room temperature in LiClO4-MeCN afforded exclusively benzophenone azines (2), whereas in NaOMe-MeOH benzophenone dimethyl acetals (3) were formed as the main products.On the other hand, the oxidation using a graphite anode in refluxing MeOH containing NaOMe gave diphenylmethyl methyl ethers (4), along with diphenylmethanes (5).When the analogous electrolysis was conducted in the presence of methacrylic acid derivatives, corresponding diphenylcyclopropanes (7) were obtained in relatively high yields.
