50844-89-8 Usage
Uses
Used in Chemical Synthesis:
4,6-Pyrimidinedicarbonitrile (9CI) is used as a chemical intermediate for the synthesis of various compounds. Its unique structure allows it to be a versatile building block in the creation of different organic molecules, particularly those with potential applications in pharmaceuticals, agrochemicals, and other industries.
Used in Research and Development:
In the field of research and development, 4,6-Pyrimidinedicarbonitrile (9CI) is utilized as a starting material for the exploration of new chemical reactions and the development of novel compounds. Its reactivity and structural properties make it an interesting candidate for studying reaction mechanisms and designing new synthetic pathways.
Used in Pharmaceutical Industry:
4,6-Pyrimidinedicarbonitrile (9CI) is used as a key component in the synthesis of certain pharmaceutical compounds. Its presence in the molecular structure can contribute to the biological activity of the final product, potentially leading to the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 4,6-Pyrimidinedicarbonitrile (9CI) is employed as a precursor for the production of various agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and agricultural productivity.
Used in Environmental Applications:
Although the potential environmental applications of 4,6-Pyrimidinedicarbonitrile (9CI) are not well-documented, it may be used in the development of compounds that can help address environmental challenges, such as pollution control or the remediation of contaminated sites. Its chemical properties could be harnessed to create new materials with specific environmental benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 50844-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,4 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50844-89:
(7*5)+(6*0)+(5*8)+(4*4)+(3*4)+(2*8)+(1*9)=128
128 % 10 = 8
So 50844-89-8 is a valid CAS Registry Number.
50844-89-8Relevant academic research and scientific papers
Fatila, Elisabeth M.,Clerac, Rodolphe,Rouzieres, Mathieu,Soldatov, Dmitriy V.,Jennings, Michael,Preuss, Kathryn E.
, p. 13298 - 13301 (2013)
A binuclear metal coordination complex of the first thiazyl-based biradical ligand 1 is reported (1 = 4,6-bis(1,2,3,5-dithiadiazolyl)pyrimidine; hfac =1,1,1,5,5,5,-hexafluoroacetylacetonato-). The Mn(hfac)2-biradical- Mn(hfac)2 complex 2 is a rare example of a discrete, molecular species employing a neutral bridging biradical ligand. It is soluble in common organic solvents and can be easily sublimed as a crystalline solid. Complex 2 has a spin ground state of ST = 4 resulting from antiferromagnetic coupling between the Sbirad = 1 biradical bridging ligand and two SMn = 5/2 MnII ions. Electrostatic contacts between atoms with large spin density promote a ferromagnetic arrangement of the moments of neighboring complexes in ribbon-like arrays. Weak antiferromagnetic coupling between these high-spin ribbons stabilizes an ordered antiferromagnetic ground state below 4.5 K. This is an unusual example of magnetic ordering in a molecular metal-radical complex, wherein the electrostatic contacts that direct the crystal packing are also responsible for providing an efficient exchange coupling pathway between molecules.
Shuvaev, Kontantin V.,Tandon, Santokh S.,Dawe, Louise N.,Thompson, Laurence K.
, p. 4755 - 4757 (2010)
Polytopic ligand design involves matching the coordination pocket composition with the metal ion coordination 'algorithm', but despite targeting [4 × 4] grids as the final outcome, metal ion preferences and ligand control can lead to widely varying complexes in the self-assembly process with Ni(ii) and Cu(ii).
