80900-33-0 Usage
Uses
Used in Pharmaceutical Industry:
1-Methoxyisoquinolin-3-aMine is used as a building block for the creation of new drug molecules for its potential as an antitumor agent and its role in neurodegenerative diseases. Its unique chemical structure and properties make it a promising candidate for the development of bioactive compounds with therapeutic applications.
Used in Medicinal Chemistry:
1-Methoxyisoquinolin-3-aMine is used as a versatile compound in medicinal chemistry for its potential to be synthesized into various bioactive compounds with wide-ranging applications. Its unique properties and chemical structure contribute to the development of innovative pharmaceuticals and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 80900-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,0 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80900-33:
(7*8)+(6*0)+(5*9)+(4*0)+(3*0)+(2*3)+(1*3)=110
110 % 10 = 0
So 80900-33-0 is a valid CAS Registry Number.
80900-33-0Relevant academic research and scientific papers
A Synthesis of Benzonaphthyridinones: an Exception to the Knorr Reaction
Deady, Leslie W.
, p. 1135 - 1138 (2007/10/02)
The reaction of 1-methoxyisoquinolin-3-amine with ethyl acetoacetate, and subsequent ring closure, is reported.Conrad-Limpach synthesis leads to the expected 4(1H)-one.The same isomer is formed under Knorr conditions (hot polyphosphoric acid), while a less acidic medium (hot acetic acid) gives the 2(1H)-one.
OXIDATION OF ALCOHOLS BY TRANSITION METAL COMPLEXES PART V. SELECTIVE CATALYTIC MONOALKYLATION OF ARYLACETONITRILES BY ALCOHOLS
Grigg, Ronald,Mitchell, Thomas R. B.,Sutthivaiyakit, Somyote,Tongpenyai, Ngampong
, p. 4107 - 4110 (2007/10/02)
Selective catalytic monoalkylation of arylacetonitriles by primary alcohols can be achieved at o using a catalyst prepared in situ from rhodium trichloride, triphenylphosphine and sodium carbonate.RuH2(PPh3)4 is a more effective catalyst for this process.
