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159326-01-9

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159326-01-9 Usage

Class

Biphenyls and derivatives

Derivative of

Biphenyl

Presence of functional groups

Ethoxy group and methyl group

Common use

Organic synthesis and as a building block for various organic compounds

Applications

Pharmaceuticals, agrochemicals, and materials science

Further research needed

Potential uses and effects on human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 159326-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,3,2 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 159326-01:
(8*1)+(7*5)+(6*9)+(5*3)+(4*2)+(3*6)+(2*0)+(1*1)=139
139 % 10 = 9
So 159326-01-9 is a valid CAS Registry Number.

159326-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethoxy-5-methylbiphenyl

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:159326-01-9 SDS

159326-01-9Downstream Products

159326-01-9Relevant articles and documents

Iodine-catalyzed tandem oxidative aromatization for the synthesis of meta-substituted alkoxybenzenes

Jiang, Dahong,Jia, Xicheng,Zhang, Shuhua,Zhang, Zhihua,Li, Lei,Qiao, Yanhui

, (2021/06/12)

A rapid method for the synthesis of meta-substituted alkoxybenzenes is achieved by oxidation of cyclohexenones. This one-pot transformation is catalyzed by molecular iodine with DDQ as an oxidant in the presence of alcohols. Diverse cyclohexenones with aryl or alkyl substitutes are well tolerated to the mild oxidative conditions affording desired products in up to 92% yield. These oxidizing processes were applicable to the efficient synthesis of useful meta-substituted phenolic products which are difficult to obtain by traditional electrophilic substitutions.

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