941294-41-3 Usage
Uses
Used in Pharmaceutical Research:
5-Bromo-4-(4-methoxyphenyl)pyrimidine is used as a building block for the synthesis of various bioactive compounds and pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
5-Bromo-4-(4-methoxyphenyl)pyrimidine is used as a key intermediate in the synthesis of complex organic molecules. Its versatile chemical properties enable the creation of a wide range of compounds for various applications.
Used in Oncology and Cancer Research:
5-Bromo-4-(4-methoxyphenyl)pyrimidine is used as an inhibitor in biological and biochemical studies, particularly in the field of oncology and cancer research. Its potential to modulate cellular processes and target specific pathways makes it a promising candidate for the development of cancer therapies.
Used in Industrial Applications:
Due to its unique chemical properties and potential pharmacological activities, 5-Bromo-4-(4-methoxyphenyl)pyrimidine has various industrial applications. It can be utilized in the development of new materials, chemical processes, and innovative products across different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 941294-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,2,9 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 941294-41:
(8*9)+(7*4)+(6*1)+(5*2)+(4*9)+(3*4)+(2*4)+(1*1)=173
173 % 10 = 3
So 941294-41-3 is a valid CAS Registry Number.
941294-41-3Relevant academic research and scientific papers
Electrophilic alkylation of arenes with 5-bromopyrimidine en route to 4-aryl-5-alkynylpyrimidines
Aksenov, Alexander V.,Domenyuk, Dmitriy A.,Magometov, Artyom Yu.,Rubin, Michael,Shcherbakov, Stanislav S.,Shcherbakova, Viktoriia Yu.,Zelensky, Vladimir A.
, p. 10315 - 10321 (2020/03/23)
A new synthetic protocol for preparation of medicinally important 4-aryl-5-alkynylpyrimidines is described. The featured approach involves a sequence of chemo- and regioselective Br?nsted acid-catalyzed electrophilic alkylation of arenes with 5-bromopyrimidine, followed by oxidative re-aromatization of the formed dihydropyrimidine ring. Finally, palladium-catalyzed Sonogashira cross-coupling reaction provided an end-game strategy.
Direct arylation of n-heteroarenes with aryldiazonium salts by photoredox catalysis in water
Xue, Dong,Jia, Zhi-Hui,Zhao, Cong-Jun,Zhang, Yan-Yan,Wang, Chao,Xiao, Jianliang
supporting information, p. 2960 - 2965 (2014/03/21)
A highly effective visible light-promoted "radical-type" coupling of N-heteroarenes with aryldiazonium salts in water has been developed. The reaction proceeds at room temperature with [Ru(bpy)3]Cl 2×6 H2O as a photosensit
