131926-77-7 Usage
Chemical Structure
It belongs to the carbazole family, which are heterocyclic aromatic compounds.
The structure includes an indole ring with a cyano group, a methoxy group, and a methyl group attached.
Biological Activities
Carbazole compounds often exhibit diverse biological activities.
Specific activities of this compound are under investigation, potentially in medicine and pharmacology.
Chemical Properties
The presence of the cyano, methoxy, and methyl groups imparts unique chemical properties.
These properties may influence its reactivity, stability, and interactions with other molecules.
Therapeutic Potential
Ongoing research aims to explore its potential as a therapeutic agent.
It may have applications in various medical and pharmacological contexts.
Biomedical Research
Scientists are actively studying this compound to understand its effects and mechanisms of action.
Investigations focus on its pharmacological properties and potential therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 131926-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,2 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131926-77:
(8*1)+(7*3)+(6*1)+(5*9)+(4*2)+(3*6)+(2*7)+(1*7)=127
127 % 10 = 7
So 131926-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H15N3O/c1-24-16-10-6-4-8-13(16)18-20(24)19-17(14(11-22)21(18)25-2)12-7-3-5-9-15(12)23-19/h3-10,23H,1-2H3
131926-77-7Relevant articles and documents
Short step syntheses of a natural product, 6-cyano-5-methoxy-12- methylindolo[2,3-a]carbazole and novel 6-aminoindolo[2,3-a]-thiazolo[5,4- c]carbazoles
Hayashi, Hiroyuki,Suzuki, Yoshiaki,Somei, Masanori
, p. 1233 - 1235 (1999)
Starting from indigo, simple synthetic methods for 6-cyano-5-methoxy- 12-methylindolo[2,3-a]carbazole and novel 6-aminoindolo[2,3-a]thiazolo-[5,4- c]carbazoles are achieved using only conventional reagents.
Combined directed Ortho and remote metalation - cross-coupling strategies. General method for benzo[a]carbazoles and the synthesis of an unnamed indolo[2,3-a]carbazole alkaloid
Cai, Xiongwei,Snieckus, Victor
, p. 2293 - 2295 (2007/10/03)
(Equation Presented) An efficient route to benzo[a]carbazoles via a metalation-cross-coupling sequence has been demonstrated (Scheme 2) and its application to the synthesis of the antitumor and antiviral alkaloid 6-cyano-5-methoxy-12-methylindolo[2,3-a]ca