166672-22-6 Usage
Uses
Used in Medicinal Chemistry:
5-(benzyloxy)pyrimidine-2-carbonitrile is used as a building block for the synthesis of other organic molecules with specific biological or pharmaceutical activities. Its pyrimidine structure and benzyloxy substituent make it a promising candidate for the development of new drugs with antiviral, antibacterial, and anticancer properties.
Used in Drug Development:
5-(benzyloxy)pyrimidine-2-carbonitrile is used as a starting material in the development of new pharmaceuticals. Its unique chemical structure allows for further functionalization and modification to enhance its biological activities and improve its therapeutic potential.
Used in Antiviral Applications:
5-(benzyloxy)pyrimidine-2-carbonitrile is used as an antiviral agent due to its potential to inhibit viral replication and reduce the severity of viral infections.
Used in Antibacterial Applications:
5-(benzyloxy)pyrimidine-2-carbonitrile is used as an antibacterial agent, showing promise in combating bacterial infections by disrupting essential cellular processes and inhibiting bacterial growth.
Used in Anticancer Applications:
5-(benzyloxy)pyrimidine-2-carbonitrile is used as an anticancer agent, with potential to target and inhibit the growth of cancer cells, making it a candidate for further research and development in oncology.
The specific properties and potential applications of 5-(benzyloxy)pyrimidine-2-carbonitrile would need to be further evaluated and studied in the laboratory to fully understand its therapeutic potential and optimize its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 166672-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,6,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 166672-22:
(8*1)+(7*6)+(6*6)+(5*6)+(4*7)+(3*2)+(2*2)+(1*2)=156
156 % 10 = 6
So 166672-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H9N3O/c13-6-12-14-7-11(8-15-12)16-9-10-4-2-1-3-5-10/h1-5,7-8H,9H2
166672-22-6Relevant academic research and scientific papers
A 5-hydroxy pyrimidine-2-carboxylic acid synthesizing method
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Paragraph 0023; 024; 0025; 0026, (2016/10/07)
The invention discloses a synthesis method for 5-hydroxyl pyrimidine-2-carboxylic acid. The synthesis method comprises the following steps: reacting 5-bromo-2-cyanopyrimidine with phenylcarbinol to generate 5-benzyloxy-2-cyanopyrimidine; then reacting5-benzyloxy-2-cyanopyrimidine in an alkaline condition, dissolving out the product by carrying out an acid adjustment on the reaction solution, and filtering and drying the dissolved solid to obtain the target compound, namely 5-hydroxyl pyrimidine-2-carboxylic acid. The synthesis method disclosed by the invention has the beneficial effects that a synthesis route for 5-hydroxyl pyrimidine-2-carboxylic acid is designed and a preparation method for the compound is provided.
SYNTHESIS AND LIQUID CRYSTAL PROPERTIES OF SUBSTITUTED 5-(ARYLCARBONYLOXY)-2-(p-CYANOPHENYL)PYRIMIDINES
Mikhaleva, M. A.,Igonina, G. A.,Savel'ev, V. A.
, p. 320 - 325 (2007/10/03)
Liquid crystal p-substituted benzoates, biphenylcarboxylates, and benzoyloxybenzoates were obtained on the basis of 5-hydroxy-2-(p-cyanophenyl)pyrimidine.The development of nematogenicity by the esters due to the p-cyanophenyl grouping was noted, and the appearance of the smectic mesophase by the variation of the ring framework of the acid fragment of the molecule was investigated.
