1261571-03-2 Usage
Description
(2-Bromo-3-iodophenyl)Methanol is a versatile chemical compound that serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is characterized by the presence of both bromine and iodine atoms, which contribute to its potential as a building block for creating diverse chemical structures. The molecule also features a hydroxyl group, which allows it to participate in reactions that require an alcohol functional group. This combination of features makes (2-Bromo-3-iodophenyl)Methanol a promising starting material for the production of a wide range of chemical products.
Uses
Used in Pharmaceutical Industry:
(2-Bromo-3-iodophenyl)Methanol is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure, containing both bromine and iodine atoms, allows for the creation of diverse chemical entities with potentially valuable properties. The presence of a hydroxyl group also enables it to participate in reactions that are crucial for the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (2-Bromo-3-iodophenyl)Methanol is utilized as a building block for the synthesis of various agrochemicals. Its ability to react with other chemicals to form new compounds with potentially beneficial properties makes it a valuable component in the development of innovative and effective products for agricultural applications.
Used in Chemical Synthesis:
(2-Bromo-3-iodophenyl)Methanol is employed as a versatile starting material in chemical synthesis. Its unique combination of bromine and iodine atoms, along with the hydroxyl group, allows it to be used in a wide range of reactions, leading to the formation of new compounds with various applications in different industries.
Used in Research and Development:
In the field of research and development, (2-Bromo-3-iodophenyl)Methanol serves as a valuable compound for exploring new chemical reactions and pathways. Its unique structure and functional groups make it an interesting subject for studying the synthesis of novel compounds and understanding the underlying chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1261571-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,5,7 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1261571-03:
(9*1)+(8*2)+(7*6)+(6*1)+(5*5)+(4*7)+(3*1)+(2*0)+(1*3)=132
132 % 10 = 2
So 1261571-03-2 is a valid CAS Registry Number.
1261571-03-2Relevant articles and documents
One-Pot Synthesis and Conformational Analysis of Six-Membered Cyclic Iodonium Salts
Caspers, Lucien D.,Spils, Julian,Damrath, Mattis,Lork, Enno,Nachtsheim, Boris J.
, p. 9161 - 9178 (2020)
Two one-pot procedures for the construction of carbon-bridged diaryliodonium triflates and tetrafluoroborates are described. Strong Br?nsted acids enable the effective Friedel-Crafts alkylation with diversely substituted o-iodobenzyl alcohol derivatives, providing diphenylmethane scaffolds, which are subsequently oxidized and cyclized to the corresponding dibenzo[b,e]iodininium salts. Based on NMR investigations and density functional theory (DFT) calculations, we could verify the so-far-undescribed existence of two stable isomers in cyclic iodonium salts substituted with aliphatic side chains in the carbon bridge.
