77664-93-8 Usage
Molecular structure
A complex chemical compound with an azulene ring, a carboxamide group, a phenyl group with a dimethylamino substitution, and an ethenyl group bonded to the phenyl ring.
Azulene ring
A seven-membered ring with five carbon atoms and two nitrogen atoms, containing a fused six-membered ring.
Carboxamide group
A functional group consisting of a carbonyl group (C=O) attached to an amide group (-CONH2).
Phenyl group
A six-membered aromatic ring with six carbon atoms and delocalized π electrons.
Dimethylamino substitution
A substituent group with two methyl groups (-CH3) attached to a nitrogen atom.
Ethenyl group
A two-carbon functional group with a carbon-carbon double bond (C=C).
Conjugated system
The presence of alternating single and double bonds in the molecule, allowing for the delocalization of electrons and increased stability.
Electron-rich molecule
The presence of electron-donating groups, such as the dimethylamino group, increases the electron density in the molecule.
Potential applications
Possible uses in pharmaceuticals, organic synthesis, and materials science due to its unique structure and properties.
Further research needed
More investigation is required to fully understand and harness the potential of 1-Azulenecarboxamide, 2-[2-[4-(dimethylamino)phenyl]ethenyl]-.
Check Digit Verification of cas no
The CAS Registry Mumber 77664-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77664-93:
(7*7)+(6*7)+(5*6)+(4*6)+(3*4)+(2*9)+(1*3)=178
178 % 10 = 8
So 77664-93-8 is a valid CAS Registry Number.
77664-93-8Relevant academic research and scientific papers
The Synthesis of 2-Styrylazulene and Its Derivatives by the Condensation of 2-Methylazulene Derivatives with Benzaldehydes
Saito, Motoyasu,Morita, Tadayoshi,Takase, Kahei
, p. 3276 - 3278 (2007/10/02)
The reaction of 2-methylazulene derivatives, such as dimethyl 2-methylazulene-1,3-dicarboxylate, methyl 3-cyano-2-methylazulene-1-carboxylate, and 1-cyano- and 1-carbamoyl-2-methylazulenes, with benzaldehyde in the presence of alkoxide resulted in condens
