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28736-47-2

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28736-47-2 Usage

Type of Compound

Synthetic chemical compound

Known for

Fluorescent properties

Common Uses

Organic electronic devices
Organic light-emitting diodes (OLEDs)
Organic photovoltaic cells

Derivative of

Anthracene (a polycyclic aromatic hydrocarbon)

Characterized by

Replacement of two hydrogen atoms in the 1 and 4 positions with fluorine atoms

Enhancement

Improved ability to emit light

Value

Component in the development of advanced optoelectronic materials

Potential Applications

Fluorescence sensing
Materials science

Unique Properties

Optical and electronic properties

Check Digit Verification of cas no

The CAS Registry Mumber 28736-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,3 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28736-47:
(7*2)+(6*8)+(5*7)+(4*3)+(3*6)+(2*4)+(1*7)=142
142 % 10 = 2
So 28736-47-2 is a valid CAS Registry Number.

28736-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-difluoroanthracene

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:28736-47-2 SDS

28736-47-2Downstream Products

28736-47-2Relevant articles and documents

Synthesis of 6,13-difluoropentacene

Tripp, Matthias W.,Koert, Ulrich

, p. 2136 - 2140 (2020)

6,13-Difluoropentacene was synthesized from 1,4-difluorobenzene. Friedel-Crafts annulation of the latter with phthalic anhydride and subsequent reduction of the anthraquinone gave 1,4-difluoroanthracene. After ortho-lithiation and reaction with phthalic anhydride a carboxylic acid was obtained whose Friedel-Crafts acylation and subsequent reductive removal of the oxygen-functionalities resulted in the formation of the target compound. The HOMO-LUMO gap of 6,13-difluoropentacene was determined via UV-vis spectroscopy and compared to other fluorinated pentacenes.

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