3254-91-9 Usage
Uses
Used in Pharmaceutical Industry:
Indenoindole is used as a drug candidate for its anti-inflammatory, anticancer, and antiviral properties. Its diverse biological activities make it a valuable compound for the development of new medications to treat various diseases and conditions.
Used in Semiconductor Industry:
Indenoindole is utilized as a semiconductor material due to its unique electronic properties. Its application in this industry contributes to the advancement of electronic devices and technologies.
Used in Organometallic Chemistry:
Indenoindole serves as a ligand in organometallic chemistry, playing a crucial role in the synthesis and stabilization of organometallic complexes. This application expands the scope of organometallic compounds and their potential uses in various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 3254-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,5 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3254-91:
(6*3)+(5*2)+(4*5)+(3*4)+(2*9)+(1*1)=79
79 % 10 = 9
So 3254-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H11N/c1-2-6-11-10(5-1)9-13-12-7-3-4-8-14(12)16-15(11)13/h1-8,16H,9H2
3254-91-9Relevant academic research and scientific papers
The Fischer indolisation reaction and the synthesis of dihydroindenoindoles
Brown, David W.,Mahon, Mary F.,Ninan, Aleyamma,Sainsbury, Malcolm,Shertzer, Howard G.
, p. 8919 - 8932 (2007/10/02)
The Fischer reaction between indanones and certain alkoxyarylhydrazines fails; the indanones are returned unreacted and the arylhydrazines are converted into the corresponding alkoxy-2-chloroarylamines and other products.A new N-amination route to arylhydrazines from the arylamines has been developed and it has been demonstrated that problems with the indolisation of alkoxyarylhydrazones can be circumvented by ring closures of their O-tosylated analogues.Some results using the Lepke synthesis of indoles are recorded.
