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2,6-difluoro-9H-fluorene is an organic compound with the molecular formula C13H8F2. It is a fluorinated derivative of the parent compound 9H-fluorene, which is a polycyclic aromatic hydrocarbon. The presence of two fluorine atoms at the 2nd and 6th positions of the fluorene core imparts unique electronic and steric properties to the molecule. 2,6-difluoro-9H-fluorene is of interest in the field of materials science, particularly for its potential applications in the synthesis of advanced polymers and electronic materials, due to the electron-withdrawing nature of fluorine atoms, which can significantly influence the electronic properties of the resulting materials. The compound is typically synthesized through various chemical reactions and can be used as a building block for more complex molecules, highlighting its importance in organic synthesis and material chemistry.

343-41-9

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343-41-9 Usage

Aromatic compound

2,6-difluoro-9H-fluorene is an aromatic compound, meaning it has a stable, planar structure with delocalized electrons.

Fluorene base

The compound is derived from a fluorene molecule, which is a tricyclic, aromatic hydrocarbon with a core structure consisting of three six-membered rings.

Fluorine substitution

Two fluorine atoms are attached to the fluorene molecule at the 2 and 6 positions, giving the compound its unique properties and reactivity.

Building block

2,6-difluoro-9H-fluorene is used as a building block in the synthesis of various organic molecules and materials, making it a versatile starting material for chemical reactions.

Industrial applications

The compound is utilized in the production of pharmaceuticals, dyes, and agrochemicals, showcasing its diverse range of applications.

Intermediate in fine chemicals manufacturing

2,6-difluoro-9H-fluorene serves as a useful intermediate in the manufacturing of fine chemicals, which are high-purity, specialized chemicals used in various industries.

Research and development

The compound is widely used in research and development in the chemical industry, highlighting its importance in the creation of new and innovative products.

Unique chemical properties

2,6-difluoro-9H-fluorene possesses unique chemical properties that contribute to its reactivity and usefulness in various chemical reactions and processes.

Valuable component

Due to its versatile applications and unique properties, 2,6-difluoro-9H-fluorene is considered a valuable component in numerous industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 343-41-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 343-41:
(5*3)+(4*4)+(3*3)+(2*4)+(1*1)=49
49 % 10 = 9
So 343-41-9 is a valid CAS Registry Number.

343-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-difluoro-9H-fluorene

1.2 Other means of identification

Product number -
Other names 2,6-Difluorfluoren

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:343-41-9 SDS

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