1005772-69-9 Usage
Uses
Used in Pharmaceutical Industry:
1-Methoxy-4-isoquinolinecarboxaldehyde is used as a research compound for the development of new pharmaceuticals, given its isoquinoline structure and potential for chemical modifications. Its presence in the aromatic heterocyclic compound category suggests that it may have properties that could be harnessed for medicinal applications.
Used in Chemical Research:
1-Methoxy-4-isoquinolinecarboxaldehyde is used as a chemical intermediate in the synthesis of various organic compounds, particularly those with potential applications in the pharmaceutical and chemical industries. Its stability and resonance characteristics make it a valuable component in the development of new chemical entities.
Used in Material Science:
Although not explicitly mentioned in the provided materials, 1-Methoxy-4-isoquinolinecarboxaldehyde's aromatic heterocyclic nature may also make it a candidate for use in material science, potentially in the development of new materials with unique properties, such as improved stability or specific reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1005772-69-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,5,7,7 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1005772-69:
(9*1)+(8*0)+(7*0)+(6*5)+(5*7)+(4*7)+(3*2)+(2*6)+(1*9)=129
129 % 10 = 9
So 1005772-69-9 is a valid CAS Registry Number.
1005772-69-9Relevant academic research and scientific papers
Sercel, Anthony D.,Sanchez, Joseph P.,Showalter, H. D. Hollis
, p. 4199 - 4208 (2007)
Synthetic routes have been developed to access 4-substituted 1(2H)-isoquinolinones from readily available precursors. This is achieved via electrophilic trapping of di- and monolithium anions derived from alkyllithium exchange of 4-bromo-1(2H)-isoquinolinones and corresponding 4-bromo-1- methoxyisoquinolines, respectively. Products derived from the latter are then hydrolyzed to the target 4-substituted 1(2H)-isoquinolinones. The methodology has potential application to access 4-substituted 1(2H)-isoquinolinones with additional substituents in either ring. Copyright Taylor & Francis Group, LLC.
SUBSTITUTED ARYLMETHYLUREAS AND HETEROARYLMETHYLUREAS, ANALOGUES THEREOF, AND METHODS USING SAME
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, (2020/07/07)
The present invention includes substituted arylmethyl ureas and heteroarylmethyl-ureas, and compositions comprising the same, that can be used to treat or prevent hepatitis B virus (HBV) infections in a patient.
