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4-methyl-2-(2-methylbutan-2-yl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34072-71-4

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34072-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34072-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,7 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34072-71:
(7*3)+(6*4)+(5*0)+(4*7)+(3*2)+(2*7)+(1*1)=94
94 % 10 = 4
So 34072-71-4 is a valid CAS Registry Number.

34072-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-(2-methylbutan-2-yl)phenol

1.2 Other means of identification

Product number -
Other names 2-tert-amyl-4-methylphenol

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:34072-71-4 SDS

34072-71-4Relevant academic research and scientific papers

Zirconia-modified superacid UDCaT-5: An efficient and versatile catalyst for alkylation reactions under solvent-free conditions

Yadav, Ganapati D.,Pathre, Ganesh S.

, p. 2684 - 2691 (2008/12/22)

UDCaT-5, a modified version of zirconia, efficiently catalyzes alkylation of phenols with alcohols under environmentally safe, heterogeneous reaction conditions with high selectivity and in excellent yields. The high content present in UDCaT-5 with preservation of tetragonal phase of zirconia was responsible for the superactivity. Several phenolic compounds carrying either electron-sulfer releasing or electron-withdrawing substituents in the ortho, meta, and para positions afforded high yields of the products. Copyright Taylor & Francis Group, LLC.

Preparation of Some 2-(2' H-Benzotriazol-2'-yl)phenol Ultraviolet Absorbers: Application of the Transalkylation Reaction

Rosevear, Judi,Wilshire, John F.K.

, p. 1163 - 1176 (2007/10/02)

When 2-(2' H-benzotriazol-2'-yl)phenols containing t-alkyl substituents are warmed in toluene solution with an aluminium chloride/nitromethane catalyst, the t-alkyl groups are transferred to the solvent (toluene).This transalkylation reaction has been used to prepare not readily accessible or previously inaccessible 2-(2' H-benzotriazol-2'-yl)phenols, a class of ultraviolet absorbers widely used in industry.

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