664302-70-9 Usage
Uses
Used in Analytical Chemistry and Biochemistry:
1-(2-Amino-1-naphthyl)isoquinoline is used as a fluorescent dye for the detection and quantification of proteins, DNA, and other biomolecules. Its high molar absorptivity and stable fluorescence signal when bound to biomolecules make it an essential tool for assays and imaging studies.
Used in Cancer Diagnosis and Treatment:
1-(2-Amino-1-naphthyl)isoquinoline is used as a potential diagnostic and therapeutic agent in cancer research. Its ability to selectively bind to tumor cells has made it a subject of interest for the development of targeted cancer treatments and diagnostic techniques.
Used in Research and Development:
1-(2-Amino-1-naphthyl)isoquinoline is used as a versatile chemical reagent in biological research, contributing to the advancement of medical diagnostics and the understanding of biomolecular interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 664302-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,4,3,0 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 664302-70:
(8*6)+(7*6)+(6*4)+(5*3)+(4*0)+(3*2)+(2*7)+(1*0)=149
149 % 10 = 9
So 664302-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H14N2/c20-17-10-9-13-5-1-3-7-15(13)18(17)19-16-8-4-2-6-14(16)11-12-21-19/h1-12H,20H2
664302-70-9Relevant academic research and scientific papers
Cu(II)-Catalyzed Construction of Heterobiaryls using 1-Diazonaphthoquinones: A General Strategy for the Synthesis of QUINOX and Related P,N Ligands
Biswas, Aniruddha,Pan, Subarna,Samanta, Rajarshi
, p. 1631 - 1636 (2022/03/14)
An efficient and straightforward method was developed for the synthesis of heterobiaryls using easily available N-oxides and diazonaphthoquinones under cheap Cu(II) catalysis. The developed method offered QUINOX and related congeners in a simple manner. A wide scope of important heterobiaryls was achieved with high site selectivity. The synthesized naphthols were transformed into the privileged related P,N ligands. Suitable resolution methods can directly afford the corresponding axially chiral heterobiaryls.
