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Azobenzene, 2,2,3,3,5,5,6,6-octafluoro-4,4-di(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65171-20-2

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65171-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65171-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65171-20:
(7*6)+(6*5)+(5*1)+(4*7)+(3*1)+(2*2)+(1*0)=112
112 % 10 = 2
So 65171-20-2 is a valid CAS Registry Number.

65171-20-2SDS

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 bis[2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl]diazene

1.2 Other means of identification

Product number -
Other names Perfluor(4,4'-dimethylazobenzol)

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:65171-20-2 SDS

65171-20-2Relevant academic research and scientific papers

Mechanochemical oxidation of fluorinated anilines to symmetric azobenzenes

Andreosso, Ivan,Papagni, Antonio,Vaghi, Luca

, p. 124 - 127 (2018/11/10)

A solventless mechanochemical methodology for the oxidation of electron-poor fluorinated anilines to the corresponding symmetrical azo compounds has been developed. In this process phenyliodine(III)diacetate and inexpensive calcium hypochlorite demonstrat

N-(POLYFLUOROARYL)-HIDROXYLAMINES. SYNTHESIS AND PROPERTIES

Miller, A.O.,Furin, G. G.

, p. 247 - 272 (2007/10/02)

Fluorine-containing N-arylhydroxylamines have been obtained by the reaction of hydroxylamine or its N- and O-derivatives on polyfluorinated benzenes and pentafluoropyridine.The influence of fluorine atoms on the reactivity of hydroxylamino group has been investigated.The reaction of N-polyflouroarylhydroxylamines with aldehydes has been shown not to occur, whereas their reaction with nitrosobenzenes leads to azoxybenzenes and with Lewis acids leads to corresponding nitrosobenzenes, azoxybenzenes and anilines.The action of acids on 2,3,5,6-tetrafluorophenylhydroxylamine leads to the acid-catalyzed rearrangement of the latter into 4-amino-2,3,5,6-tetrafluorophenol.C,N-Diarylnitrones have been obtained by the oxidation with MnO2 of fluorine-containing arylhydroxylamines possessing the CH-fragment in an α-position.

ELECTRONIC STRUCTURE AND REACTIVITY OF PHENYL AND PENTAFLUOROPHENYLSUBSTITUTED N,N-DICHLOROAMIDES AND -AMINES

Dolenko, G. N.,Zibarev, A. V.,Krupoder, S. A.,Mazalov, L. N.,Poleshchuk, O. Ch.,et al.

, p. 1 - 14 (2007/10/02)

The charge distribution in the polyfluoroaromatic N,N-dichloroamides and -amines and their hydrocarbon analogues has been established from the X-ray fluorescent CIKα- and SKα-spectra and X-ray photoelectron spectra of chlorine, sulph

Evidence for Nitrene Formation via Pyrolysis of an NN-Dihalogenoaniline: Thermal Conversion of NN-Dichloroperfluoro-p-toluidine into Perfluoro-(2-dichloromethyl-4-methylpyridine) and Perfluoro-(1-cyano-4-methylcyclopenta-1,3-diene)

Al-Saleh, Balkis A.,Banks, Ronald E.,Barlow, Michael G.

, p. 997 - 998 (2007/10/02)

Flow pyrolysis of NN-dichloroperfluoro-p-toluidine at 550 degC and ca. 1 mmHg yields, inter alia, perfluoro-4,4'-azotoluene, perfluoro-4-chlorotoluene, perfluoro-(2-dichloromethyl-4-methylpyridine) and perfluoro-(1-cyano-4-methylcyclopenta-1,3-diene); for

REACTIONS OF POLYFLUORINATED AROMATIC N,N-DICHLOROAMIDES AND N,N-DICHLOROAMINES WITH SULFUR AND SELENIUM AND THEIR ELECTRONIC STRUCTURE

Zibarev, A. V.,Dolenko, G. N.,Krupoder, S. A.,Mazalov, L. N.,Poleshchuk, O. Kh.,et al.

, p. 347 - 354 (2007/10/02)

In the reaction of the N,N-dichloroamides of pentafluorobenzenesulfonic and pentafluorobenzoic acids with sulfur and selenium the corresponding iminosulfur and iminoselenium dichlorides are formed.It was found that polyfluorinated azobenzenes are formed in the reaction of N,N-dichloroamines of the polyfluorinated aromatic series with sulfur and selenium.The charges at the chlorine atoms of polyfluorinated aromatic N,N-dichloroamides and N,N-dichloroamines were determined on the basis of data from 35Cl NQR, the x-ray fluoroscence mechanism spectra of the chlorine, and quantum-chemical calculations by the CNDO/2 method.The mechanism of the reactions of polyfluorinated aromatic N,N-dichloroamides and N,N-dichloroamines with sulfur and selenium is discussed.

SYNTHESIS AND PROPERTIES OF POLYFLUORINATED AROMATIC N,N-DICHLOROAMINES AND N-CHLOROIMINOPOLYFLUOROCHLORO-2,5-CYCLOHEXADIENES

Andreevskaya, O. I.,Markovskii, L. N.,Poleshchuk, O. Kh.,Furin, G. G.,Shermolovich, Yu. G.,Yakobson, G. G.

, p. 717 - 722 (2007/10/02)

The behaviour of 4-XC6F4NH2 (X=NO2, CN, F, H, CH3, OCH3, C4H9) in reaction with tert-butyl hypochlorite was investigated.Polyfluorinated anilines containing electron-donating substituents form N-chloroiminopolyfluorochloro-2,5-cyclohexadienes, whereas the

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