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1-(2-methylprop-2-enoxy)-4-tert-butyl-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54932-87-5

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54932-87-5 Usage

Type of compound

Benzene derivative

Structural features

A tert-butyl group attached to the benzene ring
A 2-methylprop-2-enoxy group attached to the benzene ring

Common uses

Production of solvents
Production of polymers
Production of pharmaceuticals

Stability and reactivity

High stability and reactivity

Application

Used as a precursor in organic synthesis

Research and development

Studied for potential use in the development of new materials
Liquid crystals
Nanomaterials

Significance

Plays a significant role in various industries and has potential for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 54932-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,3 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54932-87:
(7*5)+(6*4)+(5*9)+(4*3)+(3*2)+(2*8)+(1*7)=145
145 % 10 = 5
So 54932-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O/c1-11(2)10-15-13-8-6-12(7-9-13)14(3,4)5/h6-9H,1,10H2,2-5H3

54932-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tert-butyl-4-(2-methylprop-2-enoxy)benzene

1.2 Other means of identification

Product number -
Other names 4-tert-Butylphenyl 2-methyl-2-propenyl ether

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:54932-87-5 SDS

54932-87-5Relevant academic research and scientific papers

Contra-Thermodynamic Positional Isomerization of Olefins

Zhao, Kuo,Knowles, Robert R.

supporting information, p. 137 - 144 (2022/01/19)

A light-driven method for the contra-thermodynamic positional isomerization of olefins is described. In this work, stepwise PCET activation of a more substituted and more thermodynamically stable olefin substrate is mediated by an excited-state oxidant an

Nickel-catalyzed deallylation of aryl allyl ethers with hydrosilanes

Wang, Jingyang,Wang, Yu,Ding, Guangni,Wu, Xiaoyu,Yang, Liqun,Fan, Sijie,Zhang, Zhaoguo,Xie, Xiaomin

, (2021/09/28)

An efficient and mild catalytic deallylation method of aryl allyl ethers is developed, with commercially available Ni(COD)2 as catalyst precursor, simple substituted bipyridine as ligand and air-stable hydrosilanes. The process is compatible with a variety of functional groups and the desired phenol products can be obtained with excellent yields and selectivity. Besides, by detection or isolation of key intermediates, mechanism studies confirm that the deallylation undergoes η3-allylnickel intermediate pathway.

Pd-Catalyzed regioselective hydroesterification of 2-allylphenols to seven-membered lactones without external CO gas

Chang, Wenju,Li, Jingfu,Ren, Wenlong,Shi, Yian

supporting information, p. 3047 - 3052 (2016/03/19)

Effective Pd-catalyzed regioselective hydroesterification of 2-allylphenols with phenyl formate is described. A variety of seven-membered lactones can be obtained in good yields under mild conditions without the use of toxic CO gas.

Synthesis and structure of [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] and it's catalytic property towards regioselective and stereoselective allylation of phenols

Sinha, Abhilasha,Khatua, Snehadrinarayan,Bhattacharjee, Manish

supporting information, p. 116 - 120 (2015/02/19)

The compound, [Ru(PPh3)2(bipy)(MeCN)Cl][BPh4] (1) has been synthesized from the precursor complex, [Ru(bipy)(PPh3)2Cl2]. The complex has been structurally characterized. This complex has been found to be an efficient catalyst for the regioselective allylation of phenols.

OXAZOLOBENZIMIDAZOLE DERIVATIVES

-

Page/Page column 12, (2011/04/18)

The present invention is directed to oxazolobenzimidazole derivatives which are potentiators of metabotropic glutamate receptors, particularly the mGluR2 receptor, and which are useful in the treatment or prevention of neurological and psychiatric disorde

Mo(CO)6 catalyzed one-pot conversion of allyl aryl ethers to dihydrobenzofurans

Bernard, Angela M.,Cocco, Maria T.,Onnis, Valentina,Piras, Pier P.

, p. 41 - 43 (2007/10/03)

Molybdenum hexacarbonyl effectively catalyses a tandem Claisen rearrangement-cyclization reaction of allyl aryl ethers to give good yields of dihydrobenzofurans.

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