36847-10-6 Usage
Uses
Used in Pharmaceutical Industry:
4,6-DIBROMOPYRIMIDINE is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of diverse medicinal compounds with potential applications in treating a wide range of diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 4,6-DIBROMOPYRIMIDINE is utilized as a key component in the production of pesticides and other agricultural chemicals. Its incorporation into these products helps to enhance crop protection and improve overall agricultural yields.
Used in Dye Industry:
4,6-DIBROMOPYRIMIDINE is employed as a precursor in the synthesis of dyes, which are used in various applications such as textiles, plastics, and printing inks. Its presence in these dyes contributes to the colorfastness and stability of the final products.
Used in Organic Synthesis:
As a reagent in organic synthesis, 4,6-DIBROMOPYRIMIDINE is used to facilitate various chemical reactions, enabling the formation of new compounds with specific properties and applications. Its versatility in this context makes it a valuable tool for chemists working across different fields.
Used in Chemical Production:
4,6-DIBROMOPYRIMIDINE serves as an intermediate in the manufacturing process of a variety of chemicals. Its role in these processes is crucial for the successful production of end products that find use in multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 36847-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36847-10:
(7*3)+(6*6)+(5*8)+(4*4)+(3*7)+(2*1)+(1*0)=136
136 % 10 = 6
So 36847-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H2Br2N2/c5-3-1-4(6)8-2-7-3/h1-2H
36847-10-6Relevant articles and documents
Ground triplet pyrimidine-4,6-diyl bis(tert-butyl nitroxide) as a paramagnetic building block for metal-organic frameworks
Homma, Yuta,Okazawa, Atsushi,Ishida, Takayuki
, p. 3120 - 3123 (2013)
We synthesized pyrimidine-4,6-diyl bis(tert-butyl nitroxide) (pmbNO), and characterized as a biradical by means of ESR spectroscopy. The zero-field splitting parameters were |D|/hc = 2.52 × 10-2 cm-1 and |E|/hc = 2.34 × 10-3 cm-1 in frozen toluene at 100 K. Magnetic study clarified the presence of intramolecular ferromagnetic coupling with 2J/kB = +18.5(5) K in frozen toluene-ethanol. DFT calculation supports the ground triplet state of pmbNO. The reaction of pmbNO with Cu(hfac)2 gave [Cu3(pmbNO)2(hfac) 4], and the structure was determined by X-ray crystallographic analysis. Though the ligand was reduced to be an anion radical, pmbNO is confirmed to work as a rigid bridge, and the nitroxide oxygen atoms can ligate the metal ions.
Arylation of halogenated pyrimidines via a suzuki coupling reaction
Schomaker,Delia
, p. 7125 - 7128 (2007/10/03)
The Suzuki coupling reaction has been used extensively for the synthesis of a wide variety of unsymmetrical biaryl compounds. We have extended this reaction to demonstrate the utility of preparing monophenyl-, diphenyl-, or triphenylpyrimidine depending on the reaction conditions. Further, it has been shown that chloropyrimidine substrates are preferable over iodo-, bromo-, or fluoropyrimidines.
