321921-99-7 Usage
Uses
Used in Pharmaceutical Research:
5-Isoquinolinamine,8-methoxy-(9CI) is used as a research compound for its potential role in the development of new pharmaceutical agents. Its unique structure and biological activities make it a valuable candidate for exploring novel therapeutic approaches and drug discovery.
Used in Drug Synthesis:
As a chemical intermediate, 5-Isoquinolinamine,8-methoxy-(9CI) is utilized in the synthesis of various pharmaceutical compounds. Its structural properties allow it to be a key component in the creation of new drugs with potential therapeutic benefits.
Further research is necessary to fully understand the potential uses and effects of 5-Isoquinolinamine,8-methoxy-(9CI) in different applications and industries. Its current applications are primarily focused on pharmaceutical research and drug synthesis, where its unique properties and potential can be harnessed for the development of innovative treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 321921-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,9,2 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 321921-99:
(8*3)+(7*2)+(6*1)+(5*9)+(4*2)+(3*1)+(2*9)+(1*9)=127
127 % 10 = 7
So 321921-99-7 is a valid CAS Registry Number.
321921-99-7Relevant articles and documents
NAPHTHOL, QUINOLINE AND ISOQUINOLINE-DERIVED UREA MODULATORS OF VANILLOID VR1 RECEPTOR
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Page 139, (2008/06/13)
This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to naphthol, quinoline and isoquinoline-derived ureas that are potent antagonists or agonists of VR1 which are useful for the treatment and prevention of inflammatory and other pain conditions in mammals.
Synthesis of indole-4-carboxaldehydes and 4-Acetylindole from N-alkyl-5-aminoisoquinolinium salts
Muchowski
, p. 1293 - 1297 (2007/10/03)
N-Alkyl-5-aminoisoquinolinium salts (8a-d) are converted into indole-4-carboxaldehydes (1a-c) on heating in a two phase alkyl acetate-water system containing an excess of a 2:1 sodium bisulfite-sodium sulfite mixture, 4-Acetylindole 1e is prepared in the same way from 1-methyl-2-cyanomethylisoquinolinium bromide 8f.
