54198-75-3 Usage
Uses
Used in Organic Synthesis:
4-Pyrimidinemethanol, 2,6-dimethyl(9CI) is used as a building block for the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and functional groups make it a versatile compound for the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
4-Pyrimidinemethanol, 2,6-dimethyl(9CI) has potential application in the field of medicinal chemistry for the development of new drugs and therapeutics. Its pyrimidine core and functional groups can be modified to create novel compounds with potential biological activity and therapeutic benefits.
Used in Pharmaceutical Industry:
4-Pyrimidinemethanol, 2,6-dimethyl(9CI) is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups can be utilized to create new drug candidates with improved efficacy, selectivity, and safety profiles.
Used in Agrochemical Industry:
4-Pyrimidinemethanol, 2,6-dimethyl(9CI) is used as a building block for the preparation of agrochemicals, such as pesticides and herbicides. Its potential use in this industry can contribute to the development of more effective and environmentally friendly agricultural products.
Check Digit Verification of cas no
The CAS Registry Mumber 54198-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,9 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54198-75:
(7*5)+(6*4)+(5*1)+(4*9)+(3*8)+(2*7)+(1*5)=143
143 % 10 = 3
So 54198-75-3 is a valid CAS Registry Number.
54198-75-3Relevant 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.
supporting information, 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.
Studies on Pyrimidine Derivatives. XX. Synthetic Utility of Hydroxymethylpyrimidines and Related Compounds
Sakamoto, Takao,Tanji, Ken-Ichi,Niitsuma, Setsuko,Ono, Takayasu,Yamanaka, Hiroshi
, p. 3362 - 3368 (2007/10/02)
The conversion of a hydroxymethyl group at the 2- or 4-position of simple pyrimidines to a chloromethyl, cyanomethyl, ethoxycarbonylmethyl, or formyl group is described.Various pyrimidines having an olefinic side chain were also synthesized via Witting reagents derived from chloromethylpyrimidines.Keywords - hydroxymethylation; chloromethylpyrimidine; cyanomethylpyrimidine; pyrimidinecarbaldehyde; Witting reaction
