503536-75-2 Usage
Description
2-Pyridinamine,5-(4-methoxyphenyl)-(9CI) is an organic compound characterized by its yellow crystalline structure. It is a derivative of pyridinamine with a specific arrangement of functional groups, which contributes to its unique chemical properties and potential applications.
Uses
Used in Pharmaceutical Industry:
2-Pyridinamine,5-(4-methoxyphenyl)-(9CI) is used as a key intermediate compound for the preparation of various pharmaceutical agents. Its application reason lies in its unique chemical structure, which allows for the development of novel therapeutics with potential benefits in treating different health conditions.
Used in Enzyme Inhibition:
In the field of biochemistry, 2-Pyridinamine,5-(4-methoxyphenyl)-(9CI) is utilized as a precursor in the synthesis of luciferase inhibitors. These inhibitors are essential tools for studying the function and regulation of luciferase enzymes, which are involved in various biological processes.
Used in Antifungal Applications:
2-Pyridinamine,5-(4-methoxyphenyl)-(9CI) is also used as a starting material for the development of substituted triazoles, which exhibit antifungal properties. These antifungal agents are crucial in combating fungal infections and can be used in the agricultural and medical industries to protect plants and treat human diseases.
Used in Metabolite Research:
Furthermore, 2-Pyridinamine,5-(4-methoxyphenyl)-(9CI) is employed in the synthesis of PhIP (A617000) metabolites and derivatives. PhIP is a heterocyclic amine found in cooked meat products and has been linked to various health concerns. The study of its metabolites and derivatives can provide valuable insights into the mechanisms of its action and potential mitigation strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 503536-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,3 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 503536-75:
(8*5)+(7*0)+(6*3)+(5*5)+(4*3)+(3*6)+(2*7)+(1*5)=132
132 % 10 = 2
So 503536-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O/c1-15-11-5-2-9(3-6-11)10-4-7-12(13)14-8-10/h2-8H,1H3,(H2,13,14)
503536-75-2Relevant articles and documents
Recyclable Pd/CuFe2O4 nanowires: A highly active catalyst for C-C couplings and synthesis of benzofuran derivatives
Lakshminarayana, Bhairi,Chakraborty, Jhonti,Satyanarayana,Subrahmanyam, Ch.
, p. 21030 - 21039 (2018/06/13)
Pd/CuFe2O4 nanowire-catalyzed cross coupling transformations are described. Notably, these reactions showed excellent functional group tolerance. Further, the protocol is applied to a one-pot synthesis of benzofurans via a Sonogashira coupling and intramolecular etherification sequence. The catalyst was reused and found to maintain its activity and stability.
Synthesis and evaluation of the anticoccidial activity of trifluoropyrido[1,2-a]pyrimidin-2-one derivatives
Silpa, Laurence,Niepceron, Alisson,Laurent, Fabrice,Brossier, Fabien,Pénichon, Mélanie,Enguehard-Gueiffier, Cécile,Abarbri, Mohamed,Silvestre, Anne,Petrignet, Julien
, p. 114 - 120 (2015/12/18)
Screening of our chemical library to discover new molecules exhibiting in vitro activity against the invasion of host cells by Eimeria tenella revealed a lead compound with an IC50 of 15 μM. Structure-activity relationship studies were conducted with 34 newly synthesized compounds to identify more active molecules and enhance in vitro activity against the parasite. Four compounds were more effective in inhibiting MDBK cell invasion in vitro than the lead compound.
A highly active catalytic system for Suzuki-Miyaura cross-coupling reactions of aryl and heteroaryl chlorides in water
Mao, Shu-Lan,Sun, Yue,Yu, Guang-Ao,Zhao, Cui,Han, Zhi-Jun,Yuan, Jia,Zhu, Xiaolei,Yang, Qihua,Liu, Sheng-Hua
, p. 9410 - 9417 (2013/01/15)
An easily available Pd(OAc)2/(2-mesitylindenyl) dicyclohexylphosphine/Me(octyl)3N+Cl-/K 3PO4·3H2O catalytic system was developed and it shows high catalytic activity in the Suzuki-Miyaura cross-coupling reaction of a diverse array of aryl and heteroaryl chlorides in water. Notably, this catalytic system also works with ultra-low loading of the catalyst with high turnover numbers.
