13314-99-3 Usage
General Description
1-(Anilinomethyl)pyrrolidine-2,5-dione, also known as 1-((phenylamino)methyl)pyrrolidine-2,5-dione, is a chemical compound with the molecular formula C12H12N2O2. It is a pyrrolidine derivative and contains an aniline group. 1-(Anilinomethyl)pyrrolidine-2,5-dione is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and bioactive molecules. It has been studied for its potential role in the treatment of various medical conditions, including cancer and neurological disorders. Additionally, it has been investigated for its potential use as a ligand in coordination chemistry and for its antimicrobial properties. Overall, 1-(Anilinomethyl)pyrrolidine-2,5-dione is a versatile chemical compound with potential applications in various fields of science and industry.
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 articles and documents
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.
