130373-81-8 Usage
Uses
Used in Organic Chemistry Research:
3-(1,3-DIHYDRO-ISOINDOL-2-YL)-BENZOIC ACID is used as a building block for the synthesis of various pharmaceuticals and other organic compounds. Its unique structure and properties make it a valuable tool for organic chemists working on the synthesis of complex molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3-(1,3-DIHYDRO-ISOINDOL-2-YL)-BENZOIC ACID is used as a precursor in the development of drugs for various medical conditions. Its potential applications in drug discovery highlight its importance in creating new therapeutic agents.
Used as a Laboratory Reagent:
3-(1,3-DIHYDRO-ISOINDOL-2-YL)-BENZOIC ACID also serves as a reagent in chemical reactions within the laboratory setting. Its role in facilitating specific chemical transformations underscores its utility in advancing scientific research and experimentation.
Check Digit Verification of cas no
The CAS Registry Mumber 130373-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,7 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130373-81:
(8*1)+(7*3)+(6*0)+(5*3)+(4*7)+(3*3)+(2*8)+(1*1)=98
98 % 10 = 8
So 130373-81-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO2/c17-15(18)11-6-3-7-14(8-11)16-9-12-4-1-2-5-13(12)10-16/h1-8H,9-10H2,(H,17,18)
130373-81-8Relevant articles and documents
Synthesis of phthalimides, isoindolin-1-ones and isoindolines bearing aminobenzoic acids as a new fluorescent compounds
Solis-Santos, Melchor,Ordó?ez, Mario,Ochoa-Terán, Adrián,Morales-Cueto, Rodrigo,Labastida-Galván, Victoria
, (2021/03/30)
Both experimental and theoretical methods were used in order to study the fluorescent properties of nine new compounds based on phthalimides, isoindolin-1-ones and isoindolines bearing aminobenzoic acids (2-aminobenzoic acid, 3-aminobenzoic acid and 4-aminobenzoic acid), which were obtained under mild reaction conditions. The photophysical properties of all the compounds were studied by electronic absorption and fluorescence spectroscopy in methanol solutions. All compounds exhibited fluorescence emission and high quantum yields. Additionally, it was found that the intramolecular charge in these donor-acceptor systems is significantly depending on electron-withdrawing substituents at the carboxylic acid position.