1258846-87-5 Usage
Uses
Used in Organic Synthesis:
2-(benzylamino)-5-bromonicotinic acid is used as a building block for the synthesis of various organic compounds. Its unique structure and functional groups allow for the creation of a wide range of molecules with different properties and applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(benzylamino)-5-bromonicotinic acid is used as a starting material for the development of new pharmaceuticals. Its structure and functional groups can be modified to create novel compounds with potential therapeutic effects.
Used in Pharmaceutical Development:
2-(benzylamino)-5-bromonicotinic acid is used as a precursor in the synthesis of pharmaceuticals. Its unique structure and the presence of a bromine atom may impart specific chemical properties that can be exploited to develop compounds with useful pharmacological applications.
Used in Agrochemical Development:
In the agrochemical industry, 2-(benzylamino)-5-bromonicotinic acid is used as a starting material for the development of new agrochemicals. Its structure and functional groups can be modified to create compounds with potential applications in agriculture, such as pesticides or herbicides.
Further research and development of 2-(benzylamino)-5-bromonicotinic acid may lead to the discovery of novel compounds with useful pharmacological and industrial applications, expanding its use across various industries.
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 academic research and scientific papers
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.
