67620-15-9 Usage
Molecular structure
The compound has a six-carbon ring with two carbon-carbon double bonds and two carbonyl groups (C=O) attached.
Substitution
The cyclic diene compound is substituted with two bromine atoms at the 2,5 positions and two 2-methoxyphenyl amino groups at the 3,6 positions.
Aromaticity
The 2-methoxyphenyl amino groups contribute to the compound's aromaticity, as they are derived from aniline attached to an aromatic ring.
Functional groups
The compound contains carbon-carbon double bonds, carbonyl groups, and methoxy groups as its primary functional groups.
Physical state
The compound is likely a solid at room temperature, as many organic compounds with similar structures are.
Polarity
The presence of polar functional groups, such as the carbonyl and methoxy groups, may result in a polar molecule.
Reactivity
The compound may undergo various organic reactions, such as nucleophilic addition, electrophilic substitution, and condensation reactions, due to the presence of reactive functional groups.
Applications
The unique chemical structure of 2,5-Cyclohexadiene-1,4-dione, 2,5-dibromo-3,6-bis[(2-methoxyphenyl)amino]may have potential applications in organic synthesis and material science, such as in the development of new polymers, pharmaceuticals, or other advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 67620-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,2 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67620-15:
(7*6)+(6*7)+(5*6)+(4*2)+(3*0)+(2*1)+(1*5)=129
129 % 10 = 9
So 67620-15-9 is a valid CAS Registry Number.
67620-15-9Relevant academic research and scientific papers
Reaction of Amidine Phenylogous with p-Benzoquinones
El-Din, Ahmed M. Nour,Mourad, Aboul-Fetouh E.,Hassan, Alaa A.,Gomaa, Mohsen A.
, p. 1966 - 1970 (2007/10/02)
N-(4-Dimethylaminobenzylidene)anilines and N1-(4-dimethylaminophenyl)-N1,N2-diphenylformamidine reacted with tetrachloro-, tetrabromo-, and tetrafluoro-p-benzoquinones via charge-transfer complexes formation giving 2-monoa
