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5-Fluoro-2-iodophenol is a chemical compound with the molecular formula C6H4FIO. It is a derivative of phenol, containing both fluorine and iodine atoms as substituents on the aromatic ring. This unique structure and reactivity make it a valuable intermediate in the creation of various biologically active compounds.
Used in Pharmaceutical Industry:
5-Fluoro-2-iodophenol is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of biologically active compounds.
Used in Agrochemical Industry:
5-Fluoro-2-iodophenol is used as a precursor in the production of agrochemicals, playing a crucial role in the synthesis of effective and targeted chemical agents for agricultural applications.
Used in Medicinal Chemistry Research:
5-Fluoro-2-iodophenol is used as a building block in drug discovery and development within the field of medicinal chemistry, due to its potential to enhance the properties of new drug candidates.
Used in Chemical Biology Research:
5-Fluoro-2-iodophenol is utilized in chemical biology for its potential to contribute to the understanding of biological processes and the design of new bioactive molecules.
It is important to handle 5-fluoro-2-iodophenol with care, as it may pose health and environmental hazards if not used properly.

186589-87-7

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186589-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 186589-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,5,8 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 186589-87:
(8*1)+(7*8)+(6*6)+(5*5)+(4*8)+(3*9)+(2*8)+(1*7)=207
207 % 10 = 7
So 186589-87-7 is a valid CAS Registry Number.

186589-87-7SDS

SAFETY DATA SHEETS

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.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-2-iodophenol

1.2 Other means of identification

Product number -
Other names PHENOL,5-FLUORO-2-IODO

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:186589-87-7 SDS

186589-87-7Relevant academic research and scientific papers

An intra/intermolecular suzuki sequence to benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted alkenes

Carson, Matthew W.,Giese, Matthew W.,Coghlan, Michael J.

supporting information; experimental part, p. 2701 - 2704 (2009/05/26)

(Chemical Equation Presented) A route to enable the preparation of 5-benzylidenyl-benzopyridyloxepine analogues was developed to continue our research in the field of nuclear hormone receptor modulators. The key steps are1) a syn-stereoselective diboratio

Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions

Morice, Christophe,Domostoj, Mathias,Briner, Karin,Mann, André,Suffert, Jean,Wermuth, Camille-Georges

, p. 6499 - 6502 (2007/10/03)

Two intramolecular routes were experimented to reach the hexahydrobenzofuro[2,3-c]pyridine platform: a Heck and a radical reaction. The radical route was applicable to all substrates, whereas the Heck route was of limited use. The key adducts were obtained via a Mitsunobu condensation between halogenated phenols and an allylic alcohol, the 3-hydroxy-tetrahydropyridine.

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