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Phenol, 5-methoxy-2,4-bis(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62123-46-0

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62123-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62123-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,2 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62123-46:
(7*6)+(6*2)+(5*1)+(4*2)+(3*3)+(2*4)+(1*6)=90
90 % 10 = 0
So 62123-46-0 is a valid CAS Registry Number.

62123-46-0SDS

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 5-methoxy-2,4-bis(1-phenylethyl)phenol

1.2 Other means of identification

Product number -
Other names Phenol,5-methoxy-2,4-bis(1-phenylethyl)

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:62123-46-0 SDS

62123-46-0Downstream Products

62123-46-0Relevant academic research and scientific papers

Microwave-accelerated alkylation of arenes/heteroarenes with benzylic alcohols using antimony(III) chloride as catalyst: Synthesis of O-heterocycles

Shukla, Prashant,Choudhary, Manoj K.,Nayak, Sandip K.

supporting information; experimental part, p. 1585 - 1591 (2011/08/03)

An efficient protocol for alkylation of electron-rich arenes/heteroarenes with benzylic alcohols under microwave irradiation using antimony(III) chloride as catalyst has been developed. The mild reaction conditions, high yields, operational simplicity, and applicability to various substrates render the approach a useful route for the synthesis of diaryl/triarylalkane. In addition, a new route for the conversion of ortho-alkenylated phenols into functionalized O-heterocycles has been accomplished. Georg Thieme Verlag Stuttgart ? New York.

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