82104-70-9 Usage
Core structure
Isoindole-1,3(2H)-dione
The central framework of the compound, which consists of a fused benzene ring and a pyrone ring (a lactone with two carbon atoms).
Bromine atom
5-position
A bromine atom is attached to the compound at the 5th position of the isoindole core, which influences its reactivity and physical properties.
2-(2-Methoxyphenyl) substituent
2-position
A side group consisting of a 2-methoxyphenyl ring connected to the 2nd position of the isoindole core, which contributes to the compound's unique properties and reactivity.
Intermediate in synthesis
Pharmaceutical and organic compounds
The compound is mainly used as an intermediate, meaning it is a precursor in the production of other chemical compounds, particularly in the pharmaceutical and organic chemistry fields.
Biological activity
Specific drugs and molecules
Due to its unique structural properties, the compound is employed in the production of specific drugs and biologically active molecules, which can have therapeutic effects or interact with biological systems.
Laboratory and research applications
Building block for complex organic molecules
The compound can be utilized in various laboratory and research settings as a building block for the synthesis of more complex organic molecules, contributing to the development of new chemical compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 82104-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,0 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82104-70:
(7*8)+(6*2)+(5*1)+(4*0)+(3*4)+(2*7)+(1*0)=99
99 % 10 = 9
So 82104-70-9 is a valid CAS Registry Number.
82104-70-9Relevant academic research and scientific papers
Monothio- and Dithio-phthalimides: Synthesis of Dibromo-β-isoindigo Derivatives
El-Sharief, A. M. Sh.,Hammad, N.E.
, p. 1039 - 1042 (2007/10/02)
5-Bromo-3-oxo-1-thio- and 5-bromo-1,3-dithio-isoindoles (II and III) on reaction with amines either in acetic acid or under fusion give 2-aryl-1-arylimino-5-bromo-3-isoindolines (VI) and substituted 1-arylimino-5-bromo-3-thioisoindoles (VIII), respectivel
