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42244-53-1

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42244-53-1 Usage

Chemical Properties

white fine needles

Check Digit Verification of cas no

The CAS Registry Mumber 42244-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,4 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42244-53:
(7*4)+(6*2)+(5*2)+(4*4)+(3*4)+(2*5)+(1*3)=91
91 % 10 = 1
So 42244-53-1 is a valid CAS Registry Number.

42244-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-(DIDODECYLOXY)BENZENE

1.2 Other means of identification

Product number -
Other names 1,2-Bis-dodecyloxy-benzol

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:42244-53-1 SDS

42244-53-1Relevant articles and documents

Novel phenazine fused triphenylene discotic liquid crystals: synthesis, characterisation, thermal, optical and nonlinear optical properties

Gowda, Ashwathanarayana,Jacob, Litwin,Joy, Nithin,Philip, Reji,Kumar, Sandeep

, p. 19034 - 19042 (2018)

A straightforward synthesis of novel phenazine fused triphenylene discotic liquid crystals (DLCs) is realized. The condensation of 3,4-diaminobenzoic acid with a triphenylene-1,2-diquinone intermediate gives an acid derivative which upon esterification with aliphatic alcohols produces the corresponding monomeric ester derivatives of the phenazine fused triphenylene discotic liquid crystals. The intermediate acid derivative exhibits a rectangular columnar phase along with a high isotropic phase transition temperature. However, the monomeric ester derivatives show a hexagonal columnar mesophase over a broad temperature range and stable when decreased to room temperature upon cooling from the isotropic phase. The mesomorphic properties of the acid and monomeric ester derivatives of the phenazine fused triphenylene DLCs were characterised by polarised optical microscopy (POM), differential scanning calorimetry (DSC) and X-ray diffraction studies (XRD). The molecular structures of the intermediate and final compounds were characterised by spectral and elemental analysis. The photophysical properties of all the monomeric ester compounds were investigated in an anhydrous chloroform solvent and absorption bands around 291-472 nm and the corresponding emission bands at 658-661 nm were observed, respectively. The π-extended conjugation in these materials gives rise to high nonlinear optical properties. These materials have immense potential for use in electro-optical applications.

Synthesis and QCM gas-sensing properties of 3,4-dialkoxyphenyl tosylamino-substituted phthalocyanines

Harbeck, Mika,Sen, Zafer,Erbahar, Dilek D.,?elik, Esranur Fidan,Gümü?, Gülay,Musluoglu, Emel

, p. 830 - 839 (2020/01/21)

Octa-substituted metallophthalocyanines [M = Ni(II), Zn(II), Co(II), and Cu(II)] carrying 3,4-dialkoxyphenyl tosylamino groups at the peripheral positions have been synthesized from 1,2-dicyano-4,5-bis[(3,4-dialkoxyphenyl-tosylamino)methyl]benzene in the

Organic compound and 3-dimensional organic framework formed using the same

-

Paragraph 0298; 0301; 0302, (2018/07/07)

Provided is a three-dimensional organic framework. The organic framework comprises a plurality of organic molecules which are self-assembled by non-covalent bonds. Each of the organic molecules comprises: a first pair of substituents which are each bound to an aromatic ring and to immediately adjacent positions among substitutable positions of the aromatic ring; and a second pair of substituents which are each bound to immediately adjacent positions among the rest of the substitutable positions. The organic molecules are self-assembled through Van Der Waals interactions, London dispersion interactions, or hydrogen bonding between the first and second pairs of the substituents, and andpi;-andpi; interactions between the aromatic rings.COPYRIGHT KIPO 2018

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