93098-36-3 Usage
Primary Usage
Used in various pharmaceutical and chemical research applications.
Parent Compound
Ester derivative of 3-isoquinolinol.
Reactivity Enhancement
Presence of methyl and phenyl groups enhances reactivity and chemical properties.
Organic Synthesis
Commonly used as a building block in organic synthesis.
Solubility and Stability
As a methanesulfonate ester, it offers improved solubility and stability.
Drug Development
Useful in the development of new drugs and bioactive molecules.
Catalysis
Potential applications in catalysis due to its unique chemical structure and reactivity.
Material Science
Possible applications in material science due to its unique chemical structure and reactivity.
Versatility
Overall, it's a versatile compound with valuable applications in chemistry and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 93098-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,9 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93098-36:
(7*9)+(6*3)+(5*0)+(4*9)+(3*8)+(2*3)+(1*6)=153
153 % 10 = 3
So 93098-36-3 is a valid CAS Registry Number.
93098-36-3Relevant articles and documents
DIELS-ALDER REACTION OF 3(2H)-ISOQUINOLINONES, II. STUDIES OF THE LACTAM-LACTIM TAUTOMERISM OF 3(2H)-ISOQUINOLINONES
Hazai, L.,Deak, Gy.,Schnitta, A.,Hasko-Breuer, J.,Horvath, E.
, p. 303 - 313 (2007/10/02)
The literature dealing with the tautomerism of 3(2H)-isoquinolinones (3-isoquinolinols) has been surveyed.The λmax bands in the UV spectra indicating the lactam or lactim structure of the compounds prepared by us, and the main characteristics o
