870516-92-0 Usage
Uses
Used in Pharmaceutical Industry:
(2,6-dimethylpyrimidin-4-yl)methanamine is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of various biologically active compounds. Its unique structure allows it to be a key component in creating new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical field, (2,6-dimethylpyrimidin-4-yl)methanamine is utilized as an intermediate in the synthesis of agrochemicals, playing a role in the development of products designed to enhance crop protection and improve agricultural yields.
Used in Organic Synthesis:
(2,6-dimethylpyrimidin-4-yl)methanamine is employed as a building block in organic synthesis, where it can be used to construct a wide range of chemical compounds with diverse applications, from materials science to specialty chemicals.
Used in Research and Development:
(2,6-dimethylpyrimidin-4-yl)methanamine is also used in research and development settings for studying its potential applications and for the exploration of new chemical reactions and processes that can lead to innovative products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 870516-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,5,1 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 870516-92:
(8*8)+(7*7)+(6*0)+(5*5)+(4*1)+(3*6)+(2*9)+(1*2)=180
180 % 10 = 0
So 870516-92-0 is a valid CAS Registry Number.
870516-92-0Relevant academic research and scientific papers
Reaction of β-alkoxyvinyl α-ketoesters with acyclic NCN binucleophiles – Scalable approach to novel functionalized pyrimidines
Stepaniuk, Oleksandr O.,Rudenko, Tymofii V.,Vashchenko, Bohdan V.,Matvienko, Vitalii O.,Kondratov, Ivan S.,Tolmachev, Andrey A.,Grygorenko, Oleksandr O.
, p. 3472 - 3478 (2019/05/17)
Two protocols for synthesis of series of low-molecular-weight di- and tri-substituted pyrimidines bearing a functional group at the 4th position, which rely on a base-mediated condensation of amidines or guanidines with β-alkoxyvinyl α-keto esters, have been developed. This approach allowed for multigram preparation of novel pyrimidine-4-carboxylates in 21–90% yield. The synthetic utility of these compounds was demonstrated by some standard functional group transformations providing promising building blocks for organic synthesis and drug discovery.
