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1,4-Cyclohexadiene, 1,2,3,3,4,6,6-heptafluoro-5-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79150-78-0

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79150-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79150-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,5 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79150-78:
(7*7)+(6*9)+(5*1)+(4*5)+(3*0)+(2*7)+(1*8)=150
150 % 10 = 0
So 79150-78-0 is a valid CAS Registry Number.

79150-78-0SDS

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 1,2,3,3,4,6,6-heptafluoro-5-nitrocyclohexa-1,4-diene

1.2 Other means of identification

Product number -
Other names 1,4-Cyclohexadiene,1,2,3,3,4,6,6-heptafluoro-5-nitro

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:79150-78-0 SDS

79150-78-0Downstream Products

79150-78-0Relevant academic research and scientific papers

Fluorination of tetrafluorobenzenes C6HF4R with XeF2

Bardin,Shchegoleva,Frohn

, p. 153 - 159 (2007/10/03)

Replacement of hydrogen by fluorine and addition of fluorine atoms to the aromatic ring were found in the reaction of XeF2 with 1-R-2,3,4,5-tetrafluorobenzene (R = H, F, Br, NO2) or 1-R-2,3,4,6-tetrafluorobenzene (R = H, CF3) in HF or CH2Cl2-BF3·OEt2. Only fluorine addition took place in the case of 1-R-2,3,5,6-tetrafluorobenzenes (R = H, Br, CF3) or 1-Br-2,3,4,6-tetrafluorobenzene. The role of cation radicals as reactive intermediates is discusseed.

AROMATIC FLUORINE DERIVATIVES. XCIII. REACTION OF POLYFLUORINATED AROMATIC COMPOUNDS WITH XENON DIFLUORIDE IN THE PRESENCE OF HYDROGEN FLUORIDE AND SALTS OF THE XeF+MFm- (MFm-1 = SbF5, WF6) TYPE

Bardin, V. V.,Furin, G. G.,Yakobson, G. G.

, p. 525 - 530 (2007/10/02)

Under the influence of xenon difluoride in the presence of hydrogen fluoride at 20 deg C hexafluorobenzene, nitropentafluorobenzene, 4-nitroheptafluorotoluene, and octafluoronaphthalene undergo regiospecific fluorination with the formation of polyfluorinated 1,4-cyclohexadienes containing substituents other than fluorine at the C=C bond.Salts of the XeF+MFm- (MFm-1 = Sb5, WF6) type are stronger fluorinating agents and react with polyfluorinated aromatic compounds at -50 to -80 deg C.A possible reaction mechanism, involving one-electron oxidation of the polyfluorinated aromatic compounds, is discussed.

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