137769-13-2 Usage
Chemical class
Isoindolinone derivatives
The compound belongs to a group of chemical compounds that have a specific structure similar to isoindole, with a ketone group (C=O) in place of one of the carbon atoms in the ring.
3. Synthetic organic compound
The compound is artificially created through chemical reactions and does not occur naturally in the environment.
4. Potential use in pharmaceuticals and agrochemicals
The compound has potential applications in the development of new drugs and pesticides due to its unique structure and properties.
5. Building block in the synthesis of pharmaceutical compounds
The compound serves as a starting material or intermediate in the synthesis of various pharmaceutical compounds, making it an important molecule in drug discovery.
6. Biological activities
The compound has shown potential for biological activity in various studies, indicating its possible use in the development of new drugs and therapies.
7. Importance in organic chemistry and drug discovery
The compound's structure and properties make it a significant molecule for research and development in the fields of organic chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 137769-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137769-13:
(8*1)+(7*3)+(6*7)+(5*7)+(4*6)+(3*9)+(2*1)+(1*3)=162
162 % 10 = 2
So 137769-13-2 is a valid CAS Registry Number.
137769-13-2Relevant articles and documents
Influence of geometry on the emitting properties of 2,3-naphthalimides
Valat, Pierre,Wintgens, Véronique,Kossanyi, Jean,Biczók, Lászlo,Demeter, Attila,Bérces, Tibór
, p. 946 - 953 (2007/10/02)
The luminescence properties of 2,3-naphthalimides have been studied using picosecond and nanosecond spectroscopies. In acetonitrile solution N-phenyl-2,3-naphthalimide (3) is found to emit dual fluorescence with emission maxima at 385 and 490 nm, respecti
