13114-64-2 Usage
Uses
Used in Pharmaceutical Synthesis:
PYRIDIN-2-YL-UREA is utilized as a key intermediate in the development of pharmaceuticals, owing to its ability to enhance the activity and selectivity of various drug molecules. Its incorporation into drug structures can lead to improved therapeutic effects and reduced side effects, making it an essential component in the design and synthesis of novel pharmaceutical agents.
Used in Agrochemical Development:
In the agrochemical industry, PYRIDIN-2-YL-UREA serves as a crucial building block for the creation of effective and environmentally friendly pesticides and herbicides. Its unique structure allows for the design of molecules with targeted pest control properties, reducing the impact on non-target organisms and the environment.
Used in Organic Synthesis:
PYRIDIN-2-YL-UREA is employed as a versatile building block in organic synthesis, enabling the construction of a wide array of complex organic molecules. Its reactivity and compatibility with various synthetic methods make it an invaluable tool for chemists in the synthesis of natural products, pharmaceuticals, and other specialty chemicals.
Used in Metal-Catalyzed Reactions:
PYRIDIN-2-YL-UREA's ability to act as a ligand in metal-catalyzed reactions makes it a valuable component in the development of new catalytic systems. Its use in these reactions can enhance the efficiency, selectivity, and sustainability of various chemical processes, contributing to the advancement of green chemistry and sustainable chemical synthesis.
Used in Biological Systems:
The potential applications of PYRIDIN-2-YL-UREA in biological systems are currently being explored, with research focusing on its interactions with biological molecules and its potential as a modulator of biological processes. Its unique structure and reactivity may offer new opportunities for the development of bioactive compounds and the study of biological mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 13114-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13114-64:
(7*1)+(6*3)+(5*1)+(4*1)+(3*4)+(2*6)+(1*4)=62
62 % 10 = 2
So 13114-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O/c7-6(10)9-5-3-1-2-4-8-5/h1-4H,(H3,7,8,9,10)
13114-64-2Relevant articles and documents
N-(2-pyridyl)urea
Velikova,Angelova,Kossev
, p. 1273 - 1275 (1997)
The structure of the title compound, C6H7N3O, is built of layers stacked along the c axis and each layer consists of parallel zigzag ribbons of hydrogen-bonded molecules extended along the ab diagonals. Within the layers, the molecules are plane-to-plane coupled at distances of 3.330 (2) angstroms. The molecular planes from adjacent layers make an angle of 68.0 (1)°.
An efficient one-pot synthesis of industrially valuable primary organic carbamates and: N -substituted ureas by a reusable Merrifield anchored iron(ii)-anthra catalyst [FeII(Anthra-Merf)] using urea as a sustainable carbonylation source
Basu, Priyanka,Dey, Tusar Kanto,Ghosh, Aniruddha,Biswas, Surajit,Khan, Aslam,Islam, Sk. Manirul
, p. 2630 - 2643 (2020/02/20)
An efficient synthesis of primary carbamates and N-substituted ureas is explored with a newly developed heterogeneous polymer supported iron catalyst in the presence of a sustainable carbonylation source. The Merrifield anchored iron(ii)-anthra catalyst [FeII(Anthra-Merf)] was synthesized by functionalization of Merrifield polymer followed by grafting of iron metal. The catalyst [FeII(Anthra-Merf)] was characterized by several techniques, like SEM, EDAX, TGA, PXRD, XPS, FTIR, CHN, AAS and UV-Vis analysis. The designed polymer embedded [FeII(Anthra-Merf)] complex is a remarkably successful catalyst for the synthesis of primary organic carbamates and N-substituted ureas by using safe carbonylation agent urea with different derivatives of alcohols and amines, respectively. The reported catalyst is a potential candidate towards contributing a satisfactory yield of isolated products under suitable reaction conditions. The catalyst is recyclable and almost non-leaching in nature after six runs with an insignificant drop in catalytic activity. Thus we found an economical and viable catalyst [FeII(Anthra-Merf)] for primary carbamates and N-substituted urea synthesis under moderate reaction conditions.
Cyclic ureas as ortho directing substituents
Meigh,Alvarez,Joule
, p. 2012 - 2021 (2007/10/03)
Six-membered cyclic ureas are shown to have a weak ortho directing ability when linked through nitrogen to benzene and pyridine rings.
