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1,2-Ethanediol, 1,2-bis(pentafluorophenyl)-, also known as bis(pentafluorophenyl)ethane-1,2-diol, is a chemical compound characterized by its unique structure. It features a central ethane-1,2-diol moiety, which is a simple two-carbon chain with two hydroxyl groups attached to each carbon. What distinguishes 1,2-Ethanediol, 1,2-bis(pentafluorophenyl)- is the presence of two pentafluorophenyl groups, each consisting of a benzene ring with five fluorine atoms attached, which are bonded to the hydroxyl groups. This results in a highly fluorinated and symmetrical molecule. The compound is known for its stability and unique electronic properties, which can be exploited in various applications, such as in the synthesis of specialty polymers or as a ligand in coordination chemistry. chemical Its formula is C14H4F10O2, reflecting the presence of 14 carbon atoms, 4 hydrogen atoms, 10 fluorine atoms, and 2 oxygen atoms.

5267-58-3

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5267-58-3 Usage

Usage

Versatile building block in organic synthesis

Applications

Production of pharmaceuticals, agrochemicals, and materials science

Reactivity

Potential to react with a variety of other chemicals

Pentafluorophenyl groups

Enhance selectivity and protection of functional groups in organic reactions

Importance

Significant compound in the field of organic chemistry with a wide range of applications

Check Digit Verification of cas no

The CAS Registry Mumber 5267-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,6 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5267-58:
(6*5)+(5*2)+(4*6)+(3*7)+(2*5)+(1*8)=103
103 % 10 = 3
So 5267-58-3 is a valid CAS Registry Number.

5267-58-3SDS

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 2,4,5-tris(perfluorophenyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names -

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:5267-58-3 SDS

5267-58-3Downstream Products

5267-58-3Relevant academic research and scientific papers

Pentafluorophenyl carbonyl compounds in the Reformatsky-type reactions promoted with Fe(CO)5-based metal complex systems

Terent'ev,Vasil'eva,Chahovskaya,Mysova,Hambardzumyan,Kochetkov

, p. 669 - 673 (2008/12/22)

Iron pentacarbonyl is an effective promoter for additions of halogenated acid esters and nitriles to pentafluorophenyl carbonyl compounds 1, 4, and 5 by the Reformatsky-type reaction and reductive coupling of compound 1. The electron-withdrawing character

Addition of halocarboxylic acids esters and halohydrocarbons to pentafluorobenzaldehyde promoted by iron pentacarbonyl

Terent'ev,Vasil'eva,Chakhovskaya,Mysova,Kochetkov

, p. 1615 - 1618 (2007/10/03)

Iron pentacarbonyl is an efficient promoter of addition to the carbonyl group of pentafluorobenzene of alkyl α-halocarboxylates and alkyl halides. The electron-acceptor character of the pentafluorophenyl group essentially affects the course of reaction an

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