905856-70-4 Usage
Uses
Used in Pharmaceutical Research:
2-Bromo-5-iodopyrimidine is used as a building block for the production of various pharmaceutical drugs and agrochemicals. Its unique structure allows for the creation of diverse and complex molecular structures, making it a valuable tool in the development of new medications.
Used in Organic Synthesis:
2-Bromo-5-iodopyrimidine is utilized in the preparation of advanced materials and other fine chemicals. Its reactivity and the presence of both bromine and iodine atoms make it a versatile compound for creating a wide range of chemical products.
Used in Production of Pharmaceutical Drugs:
2-Bromo-5-iodopyrimidine is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique properties enable the development of innovative and effective medications for the treatment of various diseases and conditions.
Used in Agrochemical Production:
2-Bromo-5-iodopyrimidine is also used in the production of agrochemicals, contributing to the development of new and improved products for agriculture and pest control. Its versatility and reactivity make it a valuable component in the creation of effective and sustainable solutions for the agricultural industry.
Check Digit Verification of cas no
The CAS Registry Mumber 905856-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,8,5 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 905856-70:
(8*9)+(7*0)+(6*5)+(5*8)+(4*5)+(3*6)+(2*7)+(1*0)=194
194 % 10 = 4
So 905856-70-4 is a valid CAS Registry Number.
905856-70-4Relevant academic research and scientific papers
A simple Cu-catalyzed coupling approach to substituted 3-pyridinol and 5-pyrimidinol antioxidants
Nara, Susheel J.,Jha, Mukund,Brinkhorst, Johan,Zemanek, Tony J.,Pratt, Derek A.
supporting information; experimental part, p. 9326 - 9333 (2009/04/06)
(Chemical Equation Presented) A convenient approach to 3-pyridinols and 5-pyrimidinols via a two-step Cu-catalyzed benzyloxylation/catalytic hydrogenation sequence is presented. The corresponding 3-pyridinamines and 5-pyrimidinamines can be prepared in an analogous sequence utilizing benzylamine in lieu of benzyl alcohol. The radical-scavenging ability of these derivatives are preliminarily explored and reveal that the increased acidities of the pyridinols and pyrimidinols render them susceptible to more significant kinetic solvent effects when compared to phenols.
