225794-32-1 Usage
Uses
Used in Pharmaceutical Research:
(5-Bromo-4-pyrimidinyl)phenylmethanone is used as a key intermediate for the synthesis of various pharmacologically active compounds. It plays a crucial role in the development of new drugs for the treatment of a wide range of diseases.
Used in Organic Synthesis:
This chemical compound is used as a building block for the synthesis of heterocyclic compounds, which are essential in the creation of complex organic molecules with diverse applications.
Used in the Production of Fine Chemicals:
(5-Bromo-4-pyrimidinyl)phenylmethanone serves as a starting material for the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, agriculture, and materials science.
Used in the Pharmaceutical Industry:
(5-Bromo-4-pyrimidinyl)phenylmethanone is used as a valuable compound in the pharmaceutical industry for research and development purposes, contributing to the creation of innovative drugs and therapies.
Used in the Agrochemical Industry:
This versatile compound also has potential applications in the agrochemical industry, where it can be utilized in the development of new products for agricultural purposes, such as pesticides and fertilizers.
Check Digit Verification of cas no
The CAS Registry Mumber 225794-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,7,9 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 225794-32:
(8*2)+(7*2)+(6*5)+(5*7)+(4*9)+(3*4)+(2*3)+(1*2)=151
151 % 10 = 1
So 225794-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H7BrN2O/c12-9-6-13-7-14-10(9)11(15)8-4-2-1-3-5-8/h1-7H
225794-32-1Relevant articles and documents
Synthesis of 5-phenyl-10-methyl-7H-pyrimido[4,5-f][1,2,4]triazolo[4,3-a][1,4]diazepine and its evaluation as an anticonvulsant agent
Phillips, Oludotun A.,Murthy, K.S Keshava,Fiakpui, Charles Y.,Knaus, Edward E.
, p. 216 - 222 (2007/10/03)
The homolytic benzoylation (benzoyl radical) of 5-tert-butylcarbonylaminopyrimidine (6, 1 equiv.) in the presence of benzaldehyde (3 equiv.), water, sulfuric acid, and acetic acid, upon treatment with FeSO4·7H2O (3 equiv.) and 70% t-