13314-99-3 Usage
Chemical structure
A pyrrolidine derivative containing an aniline group
Synonyms
1-((phenylamino)methyl)pyrrolidine-2,5-dione
Industry use
Pharmaceutical industry as a building block for the synthesis of various drugs and bioactive molecules
Potential applications
Treatment of various medical conditions, including cancer and neurological disorders
Research areas
Coordination chemistry as a ligand and antimicrobial properties
Versatility
Wide range of potential applications in science and industry
These properties and specific content provide a comprehensive overview of 1-(Anilinomethyl)pyrrolidine-2,5-dione, highlighting its chemical structure, industry applications, and areas of research interest.
Check Digit Verification of cas no
The CAS Registry Mumber 13314-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,1 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13314-99:
(7*1)+(6*3)+(5*3)+(4*1)+(3*4)+(2*9)+(1*9)=83
83 % 10 = 3
So 13314-99-3 is a valid CAS Registry Number.
13314-99-3Relevant academic research and scientific papers
Synthesis and oxidative ring contraction of 1,5,3,7-dichalcogenadiazocanes. Novel formation of 1,2,4-diselenazolidines, 1,2,4-ditellurazolidines, and 1,2,3,4,5,7-pentathiazocanes
Takikawa, Yuji,Koyama, Yutaka,Yoshida, Takamasa,Makino, Kenshiro,Shibuya, Hiroki,Sato, Kazuto,Otsuka, Tatsuya,Shibata, Yuko,Onuma, Yuki,Aoyagi, Shigenobu,Shimada, Kazuaki,Kabuto, Chizuko
, p. 1913 - 1925 (2007/10/03)
1,5,3,7-Dithiadiazocanes, 1,5,3,7-diselenadiazocanes, and 1,5,3,7-ditelluradiazocanes were prepared from a primary amine, formalin, and H2S, NaSeH, or NaTeH, respectively. Oxidation of 1,5,3,7- diselenadiazocanes and 1,5,3,7-ditelluradiazocanes using NBS efficiently afforded 1,2,4-diselenazolidines or 1,2,4-ditellurazolidines, respectively. In contrast, treatment of 1,5,3,7-dithiadiazocanes with bromine-elemental sulfur or disulfur dichloride (S2Cl2) afforded 1,2,3,4,5,7- pentathiazocanes. An unusual oxidative conversion of 1,5,3,7- dichalcogenadiazocanes into these products was assumed to proceed through in situ formation of 1,5,3,7-dichalcogenadiazabicyclo[3.3.0]octane-type dications.
