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Phenol, 2,6-bis(1,1-dimethylethyl)-4-(3-phenyl-2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52679-02-4

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52679-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52679-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,7 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52679-02:
(7*5)+(6*2)+(5*6)+(4*7)+(3*9)+(2*0)+(1*2)=134
134 % 10 = 4
So 52679-02-4 is a valid CAS Registry Number.

52679-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-(3-phenylprop-2-enyl)phenol

1.2 Other means of identification

Product number -
Other names Phenol,2,6-bis(1,1-dimethylethyl)-4-(3-phenyl-2-propenyl)

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:52679-02-4 SDS

52679-02-4Relevant academic research and scientific papers

Electrophilic Reactivities of Vinyl p-Quinone Methides

Eitzinger, Andreas,Mayer, Robert J.,Hampel, Nathalie,Mayer, Peter,Waser, Mario,Ofial, Armin R.

, p. 2182 - 2186 (2020)

The electrophilic reactivity of a series of 8-arylated vinyl p-quinone methides (pVQMs) was determined by analyzing the kinetics of their reactions with carbanions in DMSO at 20 °C according to the linear free energy relationship log k = sN(N + E). The electrophilicity parameters E for pVQMs were used to successfully predict Michael-additions with structurally diverse C-, N-, S-, and H-nucleophiles.

Tandem 1,6-addition/cyclization/vinylcyclopropane rearrangement at low temperature under metal-free conditions: an approach to spiro[4.5]cyclohexadienones

Yuan, Zhenbo,Gai, Kuo,Wu, Youzhi,Wu, Jie,Lin, Aijun,Yao, Hequan

supporting information, p. 3485 - 3488 (2017/03/30)

A tandem 1,6-addition/cyclization/vinylcyclopropane rearrangement reaction (VCPR) of vinylogous para-quinone methides at low temperature under metal-free conditions has been disclosed for the first time. This method provides an efficient strategy for the construction of a range of spiro[4.5]cyclohexadienones in good yield, exhibiting good functional group tolerance as well as gram-scale capacity.

Process for production of 2,6-di-tert-alkenyl phenols

-

, (2008/06/13)

There is disclosed a process for the production of 2,6-di-tert-alkyl-4-alkenyl phenols wherein the improvement comprises the reaction of a 2,6-di-tert-alkyl phenol with an allyl halide to yield the 2,6-di-tert-alkyl-4-alkenyl phenol through the use of a triphase or polymer bound catalyst.

Certain cinnamyl phenols as growth inhibitors for mosquito larvae

-

, (2008/06/13)

Poly-t-butyl-cinnamyl phenols and poly-t-butyl-dihydrocinnamyl phenols are disclosed to be useful for inhibiting the growth of mosquito larvae, thus providing means for controlling mosquito populations.

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