7479-22-3 Usage
Derivative of indole
1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bisis a modified version of the heterocyclic compound indole, which is commonly found in natural products and pharmaceuticals.
Nitrophenyl group
The compound contains a 2-nitrophenyl group, which is a phenyl group with a nitro group (-NO2) attached to it.
Ethylidene bridge
The compound has an ethylidene bridge (-CH=CH-) connecting the two indole rings.
Potential applications in medicinal chemistry
1H-Indole,3,3'-[2-(2-nitrophenyl)ethylidene]bismay have potential uses in the development of new drugs or bioactive molecules.
Ongoing research
Scientists and researchers are studying the synthesis, structure, and biological activity of this compound.
Of interest to organic chemistry and drug discovery
The compound is of interest to those in the fields of organic chemistry and drug discovery due to its unique chemical and biological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 7479-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7479-22:
(6*7)+(5*4)+(4*7)+(3*9)+(2*2)+(1*2)=123
123 % 10 = 3
So 7479-22-3 is a valid CAS Registry Number.
7479-22-3Relevant articles and documents
POLYMERISATION OF INDOLE. PART 2. A NEW INDOLE TRIMER
Ishii, Hisashi,Murakami, Keiko,Sakurada(nee Kawanabe), Eri,Hosoya, Katsuhiro,Murakami, Yasuoki
, p. 2377 - 2386 (2007/10/02)
Treatment of indole (1) with toluene-p-sulphonic acid in benzene provided the 2,3'-indole trimer (4), a positional isomer of the well known 3,3'-indole trimer (3).The structure of the new trimer (4) was established by comparitive studies with the trimers (3) and (4).
