4695-86-7 Usage
Chemical structure
The compound has a complex structure containing an indole ring, a pyridinium ring, and a methoxycarbonyl group.
Heterocyclic compound
It is a heterocyclic compound, which means it contains atoms of different elements in its ring structure.
Ionic properties
The compound exhibits ionic properties due to the positively charged pyridinium moiety and a negatively charged carboxylate group.
Organic synthesis
It has potential applications in organic synthesis due to its unique structure and reactivity.
Medicinal chemistry
It may be used in medicinal chemistry as a building block for the synthesis of other complex organic molecules or as a pharmacophore in drug design.
Scientific and industrial applications
Further research may uncover additional uses for this compound in various scientific and industrial applications.
Please note that the specific content provided in the material is limited, and further research would be needed to fully understand the properties and potential applications of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 4695-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,9 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4695-86:
(6*4)+(5*6)+(4*9)+(3*5)+(2*8)+(1*6)=127
127 % 10 = 7
So 4695-86-7 is a valid CAS Registry Number.
4695-86-7Relevant articles and documents
A convenient synthesis of indole and 1,4-dihydropyridine hybrid macromolecules by dimerization of [2-(1h-indol-3-yl)ethyl]pyridinium salts
Ling, Gang,Zhang, Jing,Zhang, Rong-Zheng,Han, Fu-She
, p. 67 - 73 (2018/01/26)
The design and synthesis of a novel type of macrocyclic compounds containing indole and 1,4-dihydropyridine heterocyclic subunits is presented. The key reaction involved in the synthesis was a base-mediated dimerization of [2-(1H-indol-3-yl)ethyl]pyridinium salts. The structure of the macrocycles was unambiguously confirmed by NMR and HRMS spectroscopic and X-ray single crystal diffraction.
