850234-80-9 Usage
Uses
Used in Pharmaceutical Industry:
Pyrimidine, 2-ethenyl-4,6-dimethoxyis used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form complex molecular structures with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, pyrimidine, 2-ethenyl-4,6-dimethoxyis utilized as a precursor in the development of novel agrochemicals, contributing to the creation of effective pest control agents and plant growth regulators.
Used in Materials Science:
Pyrimidine, 2-ethenyl-4,6-dimethoxyis employed as a component in the research and development of advanced materials, leveraging its unique structural properties to enhance material performance in various applications.
Used in Organic Electronics:
pyrimidine,2-ethenyl-4,6-dimethoxyis also used as a constituent in the field of organic electronics, where its electronic properties can be harnessed to improve the efficiency and functionality of organic electronic devices such as solar cells and light-emitting diodes.
Check Digit Verification of cas no
The CAS Registry Mumber 850234-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,2,3 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 850234-80:
(8*8)+(7*5)+(6*0)+(5*2)+(4*3)+(3*4)+(2*8)+(1*0)=149
149 % 10 = 9
So 850234-80-9 is a valid CAS Registry Number.
850234-80-9Relevant academic research and scientific papers
Copper-catalyzed borylative coupling of vinylazaarenes and N-Boc imines
Smith, Joshua J.,Best, Daniel,Lam, Hon Wai
supporting information, p. 3770 - 3772 (2016/03/22)
Cu-catalyzed three-component couplings of vinylazaarenes, B2(pin)2, and N-Boc imines are described. Oxidation of the initially formed boronate gives azaarene-containing, Boc-protected amino alcohols with reasonable to good diastereoselectivities.
Enantioselective copper-catalyzed reductive coupling of alkenylazaarenes with ketones
Saxena, Aakarsh,Choi, Bonnie,Lam, Hon Wai
supporting information; experimental part, p. 8428 - 8431 (2012/08/08)
Catalytic enantioselective methods for the preparation of chiral azaarene-containing compounds are of high value. By combining the utility of copper hydride catalysis with the ability of C=N-containing azaarenes to activate adjacent alkenes toward nucleophilic additions, the enantioselective reductive coupling of alkenylazaarenes with ketones has been developed. The process is tolerant of a wide variety of azaarenes and ketones, and provides aromatic heterocycles bearing tertiary-alcohol-containing side chains with high levels of diastereo- and enantioselection.
