35252-98-3 Usage
Uses
Used in Analytical and Diagnostic Applications:
6-(Chloromethyl)-2-phenylpyrimidin-4-ol is utilized as a reagent in the generation of chemiluminescence, a process that is highly valuable in various analytical and diagnostic applications. Its ability to undergo oxidation reactions to produce a chemiluminescent compound allows for sensitive and specific detection methods in fields such as biochemistry and environmental monitoring.
Used in Organic Synthesis:
In the field of organic synthesis, 6-(Chloromethyl)-2-phenylpyrimidin-4-ol serves as a key intermediate compound, contributing to the synthesis of a range of organic molecules. Its unique structure and reactivity make it a valuable building block for the creation of new chemical entities with potential applications in various industries.
Used in Pesticide Development:
6-(Chloromethyl)-2-phenylpyrimidin-4-ol has been studied for its potential use as a pesticide, highlighting its versatility in the field of chemistry. Its chemical properties may offer new approaches to pest control, contributing to the development of more effective and environmentally friendly agricultural solutions.
Used in Pharmaceutical Research:
6-(Chloromethyl)-2-phenylpyrimidin-4-ol has also demonstrated its importance in pharmaceutical research, where it is being investigated for its potential applications in drug discovery and development. Its unique structure and reactivity may lead to the creation of new pharmaceutical agents with novel mechanisms of action, ultimately benefiting the healthcare industry.
Check Digit Verification of cas no
The CAS Registry Mumber 35252-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,5 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35252-98:
(7*3)+(6*5)+(5*2)+(4*5)+(3*2)+(2*9)+(1*8)=113
113 % 10 = 3
So 35252-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9ClN2O/c12-7-9-6-10(15)14-11(13-9)8-4-2-1-3-5-8/h1-6H,7H2,(H,13,14,15)
35252-98-3Relevant academic research and scientific papers
Chloromethyl Substituted Heterocycles from Methyl Chlorotetrolate
Janietz, D.,Goldmann, B.,Rudorf, W.-D.
, p. 607 - 616 (2007/10/02)
Reaction of amidines, isothioureas or thioureas with methyl chlorotetrolate 1 leads to pyrimidin-4-ones 2 and 1,3-thiazines (3), respectively.Compounds 2 and 3 are starting materials for the synthesis of 6-chloromethyl-uracils (4), 1,3-thiazine-2,4-dione 5 and 6-benzylthiomethyl-thiazinone (6). 2-Aminothiazoles react with the ester 1 to yield 5-chloromethyl-thiazolopyrimidin-7-ones (7).The 5-oxo isomers 8 are obtained by reaction of thiazoles with ethyl γ-chloroacetoacetate.By reaction of 2-mercaptoimidazoles and 1 or chlorotetrolic acid the condensed 1,3-thiazinones (10) result.In the latter case the intermediate 9 is isolated.It can be cyclised to 10 by heating with acetic anhydride and sulphuric acid.
