27956-40-7 Usage
General Description
2-Chloro-5-(4-chlorophenyl)pyrimidine is a chemical compound with the molecular formula C11H6Cl2N2. It is a pyrimidine derivative that contains both chlorine and phenyl groups. 2-CHLORO-5-(4-CHLOROPHENYL)PYRIMIDINE is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds, including antiviral and anticancer drugs. It is also used as an intermediate in the manufacturing of agrochemicals and for research purposes in the development of new chemical entities. The presence of both chlorine and phenyl groups in its structure makes 2-chloro-5-(4-chlorophenyl)pyrimidine an important and versatile compound for use in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 27956-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,5 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27956-40:
(7*2)+(6*7)+(5*9)+(4*5)+(3*6)+(2*4)+(1*0)=147
147 % 10 = 7
So 27956-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H6Cl2N2/c11-9-3-1-7(2-4-9)8-5-13-10(12)14-6-8/h1-6H
27956-40-7Relevant articles and documents
Substituted heterocyclic compound, and use method and use thereof
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Paragraph 0231; 0232; 0233; 0234; 0265; 0266; 0267-0269, (2016/10/08)
The invention relates to a substituted heterocyclic compound, and a use method and a use thereof. The substituted heterocyclic compound and a medicinal composition including the compound can be used to depress orexin receptors, especially an orexin-1 rece
Synthesis and biological activities of novel β-carbolines as PDE5 inhibitors
Sui, Zhihua,Guan, Jihua,Macielag, Mark J.,Jiang, Weiqin,Qiu, Yuhong,Kraft, Patricia,Bhattacharjee, Sheela,John, T. Matthew,Craig, Elizabeth,Haynes-Johnson, Donna,Clancy, Joanna
, p. 761 - 765 (2007/10/03)
A series of N2-furoyl and N2pyrimidinyl β-carbolines was discovered to possess potent inhibitory activity against PDE5. During the synthesis we developed a tandem resin quenching protocol, which allowed us to synthesize large number