53460-45-0 Usage
General Description
2,3-dioxo-N-phenyl-1-indolinecarboxamide is a chemical compound that belongs to the class of carboxamide compounds. It is also known by the chemical name N-phenyl-2,3-dioxoindoline-1-carboxamide. 2,3-dioxo-N-phenyl-1-indolinecarboxamide is a derivative of indole, which is a heterocyclic aromatic organic compound. 2,3-dioxo-N-phenyl-1-indolinecarboxamide has potential applications in the pharmaceutical industry, particularly in the development of drugs for various medical conditions. Its chemical structure and properties make it an interesting molecule for further study and potential use in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 53460-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,6 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53460-45:
(7*5)+(6*3)+(5*4)+(4*6)+(3*0)+(2*4)+(1*5)=110
110 % 10 = 0
So 53460-45-0 is a valid CAS Registry Number.
53460-45-0Relevant articles and documents
Facile synthetic approach towards vasorelaxant active 4-hydroxyquinazoline-4-carboxamides
Aziz, Marian N.,Panda, Siva S.,Shalaby, Elsayed M.,Fawzy, Nehmedo G.,Girgis, Adel S.
, p. 28534 - 28540 (2019)
A Facile synthetic approach is reported towards 4-hydroxyquinazoline-4-carboxamides 13a-i through ring expansion of 2,3-dioxoindoline-1-carboxamides 10a-c during secondary amine 11a-d nucleophilic reaction. Single crystal X-ray studies of 10c and 13d supp
An unusual polyheterocyclic diversity by the π-cyclisation of N-carbamoyliminium ion, with or without tandem N,N-acetal cleavage, from spiro(imidazolidinoquinazolinones)
Pesquet, Anthony,Daich, Adam,Coste, Servane,Van Hijfte, Luc
, p. 1389 - 1396 (2008/12/21)
Spiro(imidazolidinoquinazolinones), obtained easily in one step from 1-carbamoylisatins, are readily converted in three steps by successive N-alkylations and sodium borohydride regio-selective reduction into the corresponding hydroxyspirolactams. The latt
