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Diazene,1,2-bis[4-(octyloxy)phenyl]-, (1E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126889-66-5

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126889-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126889-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,8 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 126889-66:
(8*1)+(7*2)+(6*6)+(5*8)+(4*8)+(3*9)+(2*6)+(1*6)=175
175 % 10 = 5
So 126889-66-5 is a valid CAS Registry Number.

126889-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-di-n-octyloxyazobenzene

1.2 Other means of identification

Product number -
Other names Bis-(4-octyloxy-phenyl)-diazene

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:126889-66-5 SDS

126889-66-5Downstream Products

126889-66-5Relevant academic research and scientific papers

Molecular mechanism of anomalous increase in the helical pitch of cholesteric liquid crystals induced by achiral dopants

Kidowaki, Masatoshi,Moriyama, Masaya,Wada, Momoyo,Tamaoki, Nobuyuki

, p. 12054 - 12061 (2007/10/03)

A dopant-induced anomalous increase in the helical pitch of dicholesteryl 10,12-docosadiynedioate 1 is explained by generation of smectic clusters in the cholesteric phase where the dopants act as promoters of smectic domains. The dopants, having a mesogenic core and the proper length of alkyl chains on both their molecular sides, such as 4,4′-dialkylazobenzenes, 4,4′-dialkylazoxybenzenes and 4,4′-dialkylbiphenyls, considerably increase the pitch. However, dopants having benzene or a binaphthyl structure in the molecular center, and alkyl chain at one side of the molecules and Z-isomers of azobenzene and azoxybenzene derivatives slightly decrease the pitch by acting as impurities that decrease the transition temperature of the host. At X-ray diffraction study of the cholesterics revealed that the pitch increases with an increase in size and amount of the smectic domains induced by the appropriate dopants.

The use of thermotropic liquid crystals in organometallic chemistry. Synthesis of new mercury, silver and gold complexes with 4,4'-disubstituted azobenzenes

Vicente, Jose,Bermudez, Maria Dolores,Carrion, Francisco J.,Martinez-Nicolas, Gines

, p. 103 - 110 (2007/10/02)

Liquid crystalline 4-XC6H4N=NC6H4X-4' can be easily prepared in high yields from the corresponding anilines.In order to study the influence of metals on the thermal properties of these materials, we have obtained adducts (2) and .The silver adducts show thermotropic behaviour.Mercuriation of dialkylazobenzenes 1a-b takes place with and LiCl to give while dialkoxyazobenzenes 1c-d require to obtain . 4a-c react with NaI to give .Both chloroaryl-, 4a and 4c, and diaryl-mercurials, 5a and 5c, act readily as transmetallating agents towards in the presence of Cl to give 2-R)Cl2> .After reaction of (tht = tetrahydrothiophene) with Cl and 4b (1:2:1), (7) can be isolated.C-H activation of acetone by 6a-b leads to 2-R)Cl> .None of the complexes 4-8 shows mesomorphic behaviour. Key words: Gold; Silver; Mercury; Aryl; Transmetallation; Orthometallated complexes

Aryliminodimagnesium Reagents. XV. Condensation with Nitrobenzene. Formation of Unsymmetrical Azobenzenes Favored By Long-Chain p-Alkoxy-Substituted Reagents

Okubo, Masao,Matsuo, Koji,Yamauchi, Akira

, p. 915 - 918 (2007/10/02)

In the reaction of p-MeC6H4N(MgBr)2 with p-alkoxynitrobenzene, no effect of alkoxy chain length on the relative yields of azoxy and azo products was observed.In contrast, in the reaction of p-alkoxy-C6H4N(MgBr)2 with p-nitrotoluene, C12- and C18-alkoxyl chains led to the corresponding unsymmetrical azobenzenes in unexpectedly high yields.This result, arising from efficient condensation and deoxygenation processes, was explained in terms of cooperation of reagent molecules through their aggregation assisted by a novel tying effect of their long chains.

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