243467-63-2 Usage
Molecular Structure
1H-Indole core, chloromethyl group, and 4-fluorophenyl substituent.
Classification
Heterocyclic compound.
Usage
Building block for synthesis of pharmaceuticals, agrochemicals, and fluorescent materials.
Potential Applications
Medicinal chemistry, precursor for bioactive compounds.
Bioactivity
Antiviral, antifungal, and anticancer properties.
Research Interest
Unique structural features, valuable target for chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 243467-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,4,6 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 243467-63:
(8*2)+(7*4)+(6*3)+(5*4)+(4*6)+(3*7)+(2*6)+(1*3)=142
142 % 10 = 2
So 243467-63-2 is a valid CAS Registry Number.
243467-63-2Relevant academic research and scientific papers
Synthesis and structure-affinity relationship investigations of 5-aminomethyl and 5-carbamoyl analogues of the antipsychotic sertindole. A new class of selective α1 adrenoceptor antagonists
Balle, Thomas,Perregaard, Jens,Larsen, Anna K.,Ramirez, Martha Teresa,Soby, Karina Krojer,Liljefors, Tommy,Andersen, Kim
, p. 1065 - 1078 (2007/10/03)
A new class of selective α1 adrenoceptor antagonists derived from the antipsychotic drug sertindole is described. The most potent and selective compound 1-(2-{4-[5-aminomethyl-1-(4-fluorophenyl)-1H-indol-3-yl]-1-piperidinyl} ethyl)-2-imidazolid
5-heteroaryl substituted indoles
-
, (2008/06/13)
The present invention relates to compounds having general formula (I) as defined herein, or a pharmaceutically acceptable acid addition salt thereof. The compounds are selective α1-adrenoceptor ligands.
