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3-tert-Butyl-5-methyl-o-benzoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24456-98-2

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24456-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24456-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,5 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24456-98:
(7*2)+(6*4)+(5*4)+(4*5)+(3*6)+(2*9)+(1*8)=122
122 % 10 = 2
So 24456-98-2 is a valid CAS Registry Number.

24456-98-2SDS

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 3-tert-Butyl-5-methyl-o-benzoquinone

1.2 Other means of identification

Product number -
Other names 5-methyl-3-t-butyl-1,2-benzoquinone

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:24456-98-2 SDS

24456-98-2Relevant academic research and scientific papers

COMPOSITION OF PRODUCTS AND MECHANISM OF THE REACTION OF OZONE WITH 2,6-DI(tert-BUTYL)-4-METHYLPHENOL

Razumovskii, S. D.,Konstantinova, M. L.,Zaikov, G. E.

, p. 949 - 952 (1992)

It was shown that two series of products with opening and with preservation of the aromatic nucleus are formed in the reaction of ozone with ionol, and a mechanism was proposed for the reaction. Keywords: ozone, phenols, 2,6-di(tert-butyl)-4-methylphenol.

Inverse electron demand hetero-Diels-Alder reaction in preparing 1,4-benzodioxin from o-quinone and enamine

Zhang, Jinsong,Taylor, Chris,Bowman, Erich,Savage-Low, Leo,Lodewyk, Michael W.,Hanne, Larry,Wu, Guang

supporting information, p. 6298 - 6302 (2013/11/06)

A process for synthesizing 1,4-benzodioxin, through oxidation of a phenol to an o-quinone followed by treatment with an enamine, has been developed. Adduct stereochemistry is found to be retained via this one-pot reaction. The method uses hypervalent iodine reagent under mild conditions and is compatible with a wide scope of phenols and enamines.

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