4090-69-1 Usage
Description
3-METHOXY-1H-ISOCHROMEN-1-ONE is a chemical compound with the molecular formula C10H8O3, belonging to the isochromenone class of compounds. It is characterized by the presence of a methoxy group at the 3-position of the isochromenone ring, which may influence its chemical properties and biological activities. As a derivative of isochromenone, it has been studied for its potential as a building block in the synthesis of pharmaceuticals and other biologically active molecules.
Uses
Used in Pharmaceutical Industry:
3-METHOXY-1H-ISOCHROMEN-1-ONE is used as a building block for the synthesis of pharmaceuticals and other biologically active molecules due to its potential pharmacological activities. Its unique structure and methoxy group at the 3-position of the isochromenone ring may contribute to the development of new drugs with therapeutic benefits.
Used in Research and Development:
3-METHOXY-1H-ISOCHROMEN-1-ONE is used in research and development for studying its potential applications and effects. Further research is needed to fully understand its chemical properties, biological activities, and how it can be utilized in the creation of new pharmaceuticals and other biologically active compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 4090-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4090-69:
(6*4)+(5*0)+(4*9)+(3*0)+(2*6)+(1*9)=81
81 % 10 = 1
So 4090-69-1 is a valid CAS Registry Number.
4090-69-1Relevant articles and documents
Cava,Spangler
, p. 4550 (1967)
Synthesis and reactivity of 2,3-dihydro-1H-2,3-benzodiazepine-1,4(5H)-dione
Bihel, Frederic J.-J.,Hellal, Malik,Bourguignon, Jean-Jacques
, p. 3791 - 3796 (2008/09/17)
Based on an orthogonal protective group strategy dealing with N-protected hydrazine, we established for the first time a highly efficient synthetic pathway leading to 2,3-benzodiazepine-1,4-dione. Moreover, the versatile reactivities exhibited by this 2,3
