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1,3-Dimethyl-2-butoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56052-33-6

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56052-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56052-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,5 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56052-33:
(7*5)+(6*6)+(5*0)+(4*5)+(3*2)+(2*3)+(1*3)=106
106 % 10 = 6
So 56052-33-6 is a valid CAS Registry Number.

56052-33-6SDS

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-butoxy-1,3-dimethylbenzene

1.2 Other means of identification

Product number -
Other names -

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:56052-33-6 SDS

56052-33-6Relevant academic research and scientific papers

Synthesis and electronic properties of covalent assemblies of oligophenylenevinylene units arising from a calix[4]arene core

Gu,Ceroni,Marconi,Armaroli,Nierengarten

, p. 6432 - 6439 (2007/10/03)

Assemblies of four oligophenylenevinylene moieties arising from a calix[4]arene core, i.e., calix[4]-oligophenylenevinylenes, have been prepared by Heck-type cross-coupling reactions of styrene derivatives with a tetraiodinated cone-calix[4]arene precursor. Photophysical studies in solution have revealed that there are electronic ground state interactions between the covalently bonded OPV moieties. The absorption spectra of the calix[4]oligophenylenevinylenes are significantly different from those obtained by summing the spectra of four model units and their emission is red-shifted when compared to the corresponding model compounds. Electrochemical studies have shown that the redox processes of the four OPV subunits do not take place at the same potentials indicating also a strong electronic interaction among them in the calix[4]oligophenylenevinylenes.

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