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855836-52-1 Usage

General Description

3-Bromo-2-iodophenol is a chemical compound with the molecular formula C6H4BrIO. It is a halogenated phenol derivative, containing both bromine and iodine atoms attached to a benzene ring. 3-BROMO-2-IODOPHENOL is commonly used as a reagent in organic synthesis, specifically in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. 3-Bromo-2-iodophenol is also known for its potential application as a substrate for various catalytic reactions in organic chemistry. Additionally, it has been investigated for its potential biological activities and has shown promise as a building block for the synthesis of novel biologically active compounds. Due to its unique structure and reactivity, 3-Bromo-2-iodophenol is an important intermediate in the production of various organic compounds used in a wide range of industries.

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:
211 % 10 = 1
So 855836-52-1 is a valid CAS Registry Number.



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017


1.1 GHS Product identifier

Product name 3-Bromo-2-iodophenol

1.2 Other means of identification

Product number -
Other names 3-BROMO-2-IODOPHENOL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:855836-52-1 SDS

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.

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