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

27238-94-4

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27238-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27238-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,3 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27238-94:
(7*2)+(6*7)+(5*2)+(4*3)+(3*8)+(2*9)+(1*4)=124
124 % 10 = 4
So 27238-94-4 is a valid CAS Registry Number.

27238-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(α-ethylbenzyl)phenol

1.2 Other means of identification

Product number -
Other names 1-Phenyl-1-(4-oxy-phenyl)-propan

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:27238-94-4 SDS

27238-94-4Downstream Products

27238-94-4Relevant academic research and scientific papers

BENZYLPHENOL DERIVATIVES AS ANTIOXIDANTS FOR AUTOXIDATION OF TETRALIN.

Yamada,Nishiyama,Suzuura,Yamamura

, p. 115 - 119 (2007/10/02)

A series of 4-benzylphenols, 2-methyl-4-benzylphenols, 4-methyl-2-benzylphenols and 4-methoxy-2-benzylphenols have been prepared and evaluated as antioxidants for tetralin at 60 degree C by means of an oxygen-absorption method. Very good activities have been observed with a series of 4-methoxy-2-benzylphenols. The electrochemical oxidation potentials of these compounds were determined using linear-sweep voltammetry. The antioxidative activities were found to correlate with both the **1**3C NMR chemical shifts ( delta ) of the ipsocarbon of the OH substituents and their peak potentials (E//p).

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