7554-84-9 Usage
Description
2-(naphthalen-2-ylcarbamoyl)benzoic acid, also known as N-(2-naphthoyl)anthranilic acid, is an organic compound with the molecular formula C20H15NO3. It features a naphthalene ring and a benzoic acid group connected by a carbamoyl group, giving it unique structural and chemical properties. 2-(naphthalen-2-ylcarbamoyl)benzoic acid is a valuable entity in the realm of organic chemistry, particularly for its applications in pharmaceutical synthesis and as an intermediate in various organic reactions.
Uses
Used in Pharmaceutical Synthesis:
2-(naphthalen-2-ylcarbamoyl)benzoic acid is utilized as a key intermediate in the development and synthesis of pharmaceuticals. Its unique structure allows it to serve as a building block for creating novel drug molecules, potentially leading to the discovery of new treatments for various diseases and conditions.
Used in Organic Chemical Reactions:
In the field of organic chemistry, 2-(naphthalen-2-ylcarbamoyl)benzoic acid is employed as an intermediate in a variety of chemical reactions. Its presence can facilitate the formation of complex organic molecules, contributing to the advancement of organic synthesis and the creation of new chemical compounds with diverse applications.
Used in Drug Development:
2-(naphthalen-2-ylcarbamoyl)benzoic acid holds promise in drug development due to its potential to be incorporated into new pharmaceutical agents. Its unique structure may contribute to the design of drugs with enhanced efficacy, selectivity, and reduced side effects, making it a valuable asset in the ongoing pursuit of innovative medications.
Check Digit Verification of cas no
The CAS Registry Mumber 7554-84-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7554-84:
(6*7)+(5*5)+(4*5)+(3*4)+(2*8)+(1*4)=119
119 % 10 = 9
So 7554-84-9 is a valid CAS Registry Number.
7554-84-9Relevant articles and documents
Aza-DielsAlder reaction between N-aryl-1-oxo-1H-isoindolium ions and tert-enamides: Steric effects on reaction outcome
Jha, Amitabh,Chou, Ting-Yi,ALJaroudi, Zainab,Ellis, Bobby D.,Cameron, T. Stanley
supporting information, p. 848 - 857 (2014/05/06)
The synthesis of 5-substituted 6,6a-dihydroisoindolo[2,1-a]quinolin-11(5H)- ones via [4 + 2] imino-DielsAlder cyclization from N-aryl-3- hydroxyisoindolinones and N-vinyl lactams under Lewis acid-catalysed anhydrous conditions is reported. Reactions of N-(2-substituted-aryl)-3- hydroxyisoindolinones with N-vinylpyrrolidone under identical conditions resulted in the formation of 2-(2-substitued-aryl)-3-(2-(2-oxopyrrolidin-1-yl) vinyl)isoindolin-1-one analogues indicating steric hinderance as the cause of deviation. The probable mechanism of the reaction based on the results from X-ray crystallography and molecular modelling is discussed.
