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1568-74-7

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1568-74-7 Usage

Type of compound

Terphenyl (aromatic hydrocarbon with three phenyl groups)

Functional groups

Two methoxy (CH3O-) groups

Position of functional groups

4 and 4'' positions of the molecule

Applications

a. Production of liquid crystals
b. Dyes
c. Organic light-emitting diodes (OLEDs)
d. Fluorophore in fluorescence microscopy
e. Chemical intermediate in organic synthesis

Industrial and scientific value

Valuable component in various applications due to its unique structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 1568-74-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1568-74:
(6*1)+(5*5)+(4*6)+(3*8)+(2*7)+(1*4)=97
97 % 10 = 7
So 1568-74-7 is a valid CAS Registry Number.

1568-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4''-DIMETHOXY-(1,1',3',1'')TERPHENYL

1.2 Other means of identification

Product number -
Other names 1,3-bis(4-methoxyphenyl)benzene

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:1568-74-7 SDS

1568-74-7Relevant articles and documents

Metal-free and solvent-free synthesis of: M -terphenyls through tandem cyclocondensation of aryl methyl ketones with triethyl orthoformate

Gan, Zongjie,Jiang, Wengao,Luo, Juan,Tang, Qiang,Xiao, Xiaoqin

, p. 12113 - 12118 (2020)

Reported here is a novel cyclocondensation of aryl methyl ketones and triethyl orthoformate for the simple synthesis of m-terphenyls. In the presence of a catalytic amount of TfOH, alkyl- and chloro-substituted acetophenones produced a series of terphenyls through a tandem reaction which merged six steps into a one-pot procedure. Moreover, the corresponding ester products were obtained when using other substituted acetophenones as the starting materials under the same reaction conditions.

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