855836-52-1 Usage
Description
3-Bromo-2-iodophenol, with the molecular formula C6H4BrIO, is a halogenated phenol derivative featuring both bromine and iodine atoms attached to a benzene ring. This unique structure endows it with distinctive reactivity and makes it a valuable intermediate in the synthesis of a variety of organic compounds.
Uses
Used in Organic Synthesis:
3-Bromo-2-iodophenol is utilized as a reagent in organic synthesis for the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its presence of both bromine and iodine atoms allows for versatile reactions and the creation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Bromo-2-iodophenol is used as a key intermediate for the synthesis of various organic compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
3-Bromo-2-iodophenol is employed as a building block in the agrochemical sector, aiding in the production of compounds that can be used in the development of pesticides and other agricultural chemicals.
Used in Catalytic Reactions:
3-Bromo-2-iodophenol is recognized for its potential application as a substrate in various catalytic reactions within organic chemistry, facilitating the synthesis of complex organic molecules.
Used in Biological Research:
It has been investigated for its potential biological activities, showing promise as a precursor for the synthesis of novel biologically active compounds, which could lead to advancements in medicine and other biological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 855836-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,8,3 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 855836-52:
(8*8)+(7*5)+(6*5)+(5*8)+(4*3)+(3*6)+(2*5)+(1*2)=211
211 % 10 = 1
So 855836-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BrIO/c7-4-2-1-3-5(9)6(4)8/h1-3,9H
855836-52-1Relevant articles and documents
An Efficient and Modular Route to C 3?-TunePhos-Type Ligands
Deng, Xu,Guan, Yu-Qing,Huo, Ning-Ning,Wang, Ya-Jing,Lv, Hui,Zhang, Xu-Mu
, p. 3726 - 3730 (2017)
An efficient and modular synthetic route to the bidentate C 3?-TunePhos was developed, which allowed tunable steric and electronic effects of the ligands. This novel chemical technology highlights a versatile C 3?-dibromodiphenyl int
Twofold unsymmetrical C-H functionalization of PyrDipSi-substituted arenes: A general method for the synthesis of substituted meta-halophenols
Sarkar, Dhruba,Melkonyan, Ferdinand S.,Gulevich, Anton V.,Gevorgyan, Vladimir
, p. 10800 - 10804 (2013/10/22)
And the world is your oyster Sequential halogenation/oxygenation reactions of 2-diisopropylsilylpyrimidine-substituted arenes provide a general and efficient synthesis of substituted meta-halophenols from simple aryl iodides (see scheme; Piv=pivaloyl). The products are poised to undergo diverse C-C, C-N, and C-O bond-forming reactions that enable the transformation of their framework and the introduction of valuable functionalities. Copyright
Synthesis of 4-functionalized-1H-indoles from 2,3-dihalophenols
Sanz, Roberto,Guilarte, Veronica,Garcia, Nuria
supporting information; experimental part, p. 3860 - 3864 (2010/09/17)
A new synthesis of 4-halo-1H-indoles has been developed from easily available 2,3-dihalophenol derivatives. The key steps are Smiles rearrangement and a one-pot or stepwise Sonogashira coupling/NaOH-mediated cyclization. Subsequent functionalization allows access to a wide variety of 2,4- or 2,3,4-regioselectively functionalized indoles.
