6321-16-0 Usage
Uses
Used in Organic Synthesis:
2-(2-bromoethyl)-5-nitro-1H-isoindole-1,3(2H)-dione is used as a building block for the synthesis of more complex organic molecules. Its structural features and functional groups facilitate the creation of a wide range of chemical entities, making it a valuable component in the field of organic chemistry.
Used in Pharmaceutical Development:
Due to its potential biological activity, 2-(2-bromoethyl)-5-nitro-1H-isoindole-1,3(2H)-dione is used as a starting material in drug development. Its chemical properties may contribute to the discovery of new therapeutic agents, particularly in the context of its possible interactions with biological targets.
Used in Materials Science:
2-(2-bromoethyl)-5-nitro-1H-isoindole-1,3(2H)-dione is used as a reagent in the design and synthesis of new materials with specific properties. Its structural features can be leveraged to create materials with tailored characteristics for applications in various industries, such as electronics, coatings, or advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 6321-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6321-16:
(6*6)+(5*3)+(4*2)+(3*1)+(2*1)+(1*6)=70
70 % 10 = 0
So 6321-16-0 is a valid CAS Registry Number.
6321-16-0Relevant academic research and scientific papers
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.
