1258846-87-5 Usage
General Description
2-(benzylamino)-5-bromonicotinic acid is a chemical compound with the molecular formula C13H11BrN2O2. It is a derivative of nicotinic acid and consists of a benzylamine group attached to the 2-position and a bromine atom attached to the 5-position of the nicotinic acid core structure. 2-(benzylamino)-5-bromonicotinic acid has potential applications in the field of organic synthesis and medicinal chemistry. Its unique structure and functional groups make it a valuable building block for the synthesis of various pharmaceuticals and agrochemicals. Additionally, the presence of a bromine atom in its structure may impart specific chemical properties that could be exploited for various purposes. Further research and development of 2-(benzylamino)-5-bromonicotinic acid may lead to the discovery of novel compounds with useful pharmacological and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1258846-87-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,8,4 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1258846-87:
(9*1)+(8*2)+(7*5)+(6*8)+(5*8)+(4*4)+(3*6)+(2*8)+(1*7)=205
205 % 10 = 5
So 1258846-87-5 is a valid CAS Registry Number.
1258846-87-5Relevant articles and documents
Synthesis of pyridodiazepinediones by using the ugi multicomponent reaction
Van Den Bogaert, An M.,Nelissen, Jo,Ovaere, Margriet,Van Meervelt, Luc,Compernolle, Frans,De Borggraeve, Wim M.
supporting information; experimental part, p. 5397 - 5401 (2010/11/18)
Benzodiazepines show a broad spectrum of biological activities. In an ongoing effort to extend molecular diversity in this type of systems, we developed a strategy for synthesizing 3,4-dihydro-1H-pyrido[2,3-e][1,4] diazepine-2,5-dione compounds starting from 2-hydroxynicotinic acid and by using an Ugi reaction as a key step in the synthesis. We opted to use 2isocyanophenyl benzoate instead of Armstrong's convertible isocyanide in this multicomponent reaction.
