25243-23-6 Usage
Uses
Used in Organic Synthesis:
N,N-di(prop-2-en-1-yl)propanamide serves as a reagent or intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities with potential applications across different industries.
Used in Pharmaceutical Production:
In the pharmaceutical industry, N,N-di(prop-2-en-1-yl)propanamide is utilized as a key component in the production of medicines, highlighting its importance in the development of therapeutic agents.
Used in Agrochemical Development:
N,N-di(prop-2-en-1-yl)propanamide also plays a role in the agrochemical sector, where it is employed in the synthesis of substances designed to enhance crop protection and improve agricultural yields.
Used in Polymer and Material Science:
N,N-di(prop-2-en-1-yl)propanamide contributes to the field of polymer science, where it is involved in the synthesis of polymers and other materials, potentially leading to innovations in material technology.
Used as a Building Block in Industrial Applications:
Recognized for its potential in various industrial applications, N,N-di(prop-2-en-1-yl)propanamide is often used as a building block in the development of new chemical compounds, showcasing its adaptability and significance in chemical research and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 25243-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,4 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25243-23:
(7*2)+(6*5)+(5*2)+(4*4)+(3*3)+(2*2)+(1*3)=86
86 % 10 = 6
So 25243-23-6 is a valid CAS Registry Number.
25243-23-6Relevant academic research and scientific papers
Direct catalytic enantio- and diastereoselective aldol reaction of thioamides
Iwata, Mitsutaka,Yazaki, Ryo,Chen, I-Hon,Sureshkumar, Devarajulu,Kumagai, Naoya,Shibasaki, Masakatsu
supporting information; experimental part, p. 5554 - 5560 (2011/05/14)
A direct catalytic asymmetric aldol reaction of thioamides using a soft Lewis acid/hard Bronsted base cooperative catalyst comprising (R,R)-Ph-BPE/[Cu(CH3CN)4]PF6/LiOAr is described. Exclusive enolate generation from thioa
