107718-34-3 Usage
Uses
Used in Pharmaceutical Industry:
4-[(4,6-DIMETHYLPYRIMIDIN-2-YL)THIO]PHENOL is used as an active pharmaceutical ingredient for its potential biological activities, contributing to the development of new medications for various therapeutic areas.
Used in Agricultural Chemicals Industry:
4-[(4,6-DIMETHYLPYRIMIDIN-2-YL)THIO]PHENOL is used as a key component in the formulation of pesticides and herbicides, leveraging its chemical properties to enhance crop protection and yield.
Used in Research and Development:
4-[(4,6-DIMETHYLPYRIMIDIN-2-YL)THIO]PHENOL serves as a valuable compound in scientific research, particularly in medicinal chemistry, for exploring its potential applications and optimizing its properties for specific uses.
Used in Industrial Applications:
Beyond its pharmaceutical and agricultural uses, 4-[(4,6-DIMETHYLPYRIMIDIN-2-YL)THIO]PHENOL is employed in various other industries, capitalizing on its unique chemical structure and properties for diverse purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 107718-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,1 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107718-34:
(8*1)+(7*0)+(6*7)+(5*7)+(4*1)+(3*8)+(2*3)+(1*4)=123
123 % 10 = 3
So 107718-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2OS/c1-8-7-9(2)14-12(13-8)16-11-5-3-10(15)4-6-11/h3-7,15H,1-2H3
107718-34-3Relevant academic research and scientific papers
Process for making phenylthiopyrimidines
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, (2008/06/13)
A process for the preparation of phenylthiopyrimidines which comprises: (a) reacting a thiopyrimidine; with sulfuryl chloride in the presence of a suitable solvent to form the sulfenyl chloride of said thiopyrimidine; (b) reacting said sulfenyl chloride of said thiopyrimidine with a phenol or substituted phenol, optionally in the presence of a Friedal-Crafts catalyst, to form a thiopyrimidinyl phenol; and (c) reacting said thiopyrimidinylphenol formed in step (b) with a base and an alkylating agent to form the end product.
