140715-56-6 Usage
Description
2-(3-BROMOPROPYL)-5-NITROISOINDOLINE-1,3-DIONE is a chemical compound characterized by the presence of a nitro group and a bromopropyl chain attached to an isoindoline-1,3-dione ring system. This unique structure endows it with potential applications in various fields, including organic synthesis, pharmaceutical research, and material science. 2-(3-BROMOPROPYL)-5-NITROISOINDOLINE-1,3-DIONE's properties, such as the presence of the nitro group and the bromopropyl chain, suggest possible antibacterial or antifungal activities and utility in cross-coupling reactions for the synthesis of complex molecules. Furthermore, the isoindoline-1,3-dione core is a common feature in bioactive compounds, hinting at the compound's potential pharmacological activity.
Uses
Used in Organic Synthesis:
2-(3-BROMOPROPYL)-5-NITROISOINDOLINE-1,3-DIONE is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure, including the nitro group and the bromopropyl chain, makes it a valuable component in the synthesis process.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(3-BROMOPROPYL)-5-NITROISOINDOLINE-1,3-DIONE is used as a potential precursor for the development of new drugs. The presence of the nitro group suggests it may have antibacterial or antifungal properties, while the isoindoline-1,3-dione core indicates possible pharmacological activity. Further research is required to explore its full potential in drug discovery.
Used in Material Science Research:
2-(3-BROMOPROPYL)-5-NITROISOINDOLINE-1,3-DIONE is also utilized in material science research for the development of new materials with unique properties. Its chemical structure, including the bromopropyl chain, may contribute to the creation of materials with specific characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 140715-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,7,1 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 140715-56:
(8*1)+(7*4)+(6*0)+(5*7)+(4*1)+(3*5)+(2*5)+(1*6)=106
106 % 10 = 6
So 140715-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BrN2O4/c12-4-1-5-13-10(15)8-3-2-7(14(17)18)6-9(8)11(13)16/h2-3,6H,1,4-5H2
140715-56-6Relevant articles and documents
A new series of N2-substituted-5-(p-toluenesulfonylamino)phthalimide analogues as α-glucosidase inhibitors
Bian, Xiaoli,Wang, Qian,Ke, Changhu,Zhao, Guilan,Li, Yiping
, p. 2022 - 2026 (2013/04/24)
Several members of a new family of non-sugar-type α-glycosidase inhibitors, bearing a 5-(p-toluenesulfonylamino)phthalimide moiety and various substituent at the N2 position, were synthesized and their activities were investigated. The newly synthesized compounds displayed different inhibition profile towards yeast α-glycosidase and rat intestinal α-glycosidase. Almost all the compounds had strong inhibitory activities against yeast α-glycosidase. Regarding rat intestinal α-glycosidase, only analogs with N2-aromatic substituents displayed varying degrees of inhibitory activities on rat intestinal maltase and lactase and nearly all compounds showed no inhibition against rat intestinal α-amylase. Structure-activity relationship studies indicated that 5-(p- toluenesulfonylamino)phthalimide moiety is a favorable scaffold to exert the α-glucosidase inhibitory activity and substituents at the N2 position have considerable influence on the efficacy of the inhibition activities.
