13314-95-9 Usage
Description
1-(piperidin-1-ylmethyl)pyrrolidine-2,5-dione, also known as N-((piperidin-1-yl)methyl)succinimide, is a chemical compound characterized by its molecular formula C11H17NO2. It is a cyclic amide derivative featuring a pyrrolidone ring and a piperidine ring. 1-(piperidin-1-ylmethyl)pyrrolidine-2,5-dione is recognized for its utility in the synthesis of a wide range of pharmaceuticals and organic compounds, making it a valuable asset in the chemical and pharmaceutical industries.
Uses
Used in Pharmaceutical Industry:
1-(piperidin-1-ylmethyl)pyrrolidine-2,5-dione is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows for the creation of new compounds with potential therapeutic benefits, contributing to drug discovery and development.
Used in Agrochemical Production:
In the agrochemical industry, 1-(piperidin-1-ylmethyl)pyrrolidine-2,5-dione is utilized as a key component in the development of novel compounds with applications in agriculture, such as pesticides and herbicides, enhancing crop protection and yield.
Used in Specialty Chemicals:
1-(piperidin-1-ylmethyl)pyrrolidine-2,5-dione also finds use in the production of specialty chemicals, where its distinctive properties can be leveraged to create tailored products for specific industrial applications, further expanding its utility and relevance in the chemical sector.
Check Digit Verification of cas no
The CAS Registry Mumber 13314-95-9 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 13314-95:
(7*1)+(6*3)+(5*3)+(4*1)+(3*4)+(2*9)+(1*5)=79
79 % 10 = 9
So 13314-95-9 is a valid CAS Registry Number.
13314-95-9Relevant articles and documents
Solvent-free preparation of monoacylaminals assisted by microwave irradiation
Sharifi,Mohsenzadeh,Naimi-Jamal
, p. 394 - 396 (2007/10/03)
Reaction of amide 1, aldehyde 2, and amine 3 promoted by microwave irradiation produced monoacylaminals 4 up to 100% yield in a short time under solvent-free conditions.
