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Diazene, bis(pentafluoroethyl)-, also known as 1,2-bis(pentafluoroethyl)hydrazine, is a chemical compound with the molecular formula C4F10H4N2. It is a colorless liquid with a pungent odor and is considered a highly reactive and potentially hazardous substance. Diazene, bis(pentafluoroethyl)- is characterized by its two pentafluoroethyl groups attached to a central hydrazine molecule, which consists of two nitrogen atoms bonded to two hydrogen atoms. Due to its reactivity, it is primarily used in the synthesis of various fluorinated compounds and as an intermediate in the production of pharmaceuticals and agrochemicals. However, it requires careful handling and storage due to its potential to form explosive decomposition products and its toxicity.

756-00-3

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756-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 756-00-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 756-00:
(5*7)+(4*5)+(3*6)+(2*0)+(1*0)=73
73 % 10 = 3
So 756-00-3 is a valid CAS Registry Number.

756-00-3SDS

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(1,1,2,2,2-pentafluoroethyl)diazene

1.2 Other means of identification

Product number -
Other names Dekafluor-azoaethan

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:756-00-3 SDS

756-00-3Relevant academic research and scientific papers

Reaction of N-Chloro-N-fluoroperhaloalkylamines with Mercury. Facile Synthesis of N-Fluoro Imines and N-Fluoro Amines

Sekiya, Akira,DesMarteau, Darryl D.

, p. 1277 - 1280 (2007/10/02)

The reaction of N-chloro-N-fluoroalkylamines with mercury has been studied with ClCF2NClF, CF3NClF, CF3CF2NClF, CF3CF2CF2NClF, and (CF2NClF)2.In the absence of solvents, all but CF3NClF undergo dehalogenation to form the corresponding N-fluoro imines in good yield.Only the syn isomers of CF3CF=NF, CF3CF2CF=NF, and (CF=NF)2 are observed.With trifluoroacetic acid as a solvent, the reactions with mercury yield the corresponding N-fluoro amines ClCF2NHF, CF3NHF, CF3CF2NHF, and CF3CF2CF2NHF in excellent yields except with (CF2NClF)2.For the latter, the amine (CF2NHF)2eliminates HF under the reaction conditions, and only (CF=NF)2 is isolated.With trifluoroacetic anhydride as a solvent, ClCF2NClF is dehalogenated with mercury to give excellent yields of CF2=NF in the first practical synthesis of this simplest perfluoro imine.Details of these reactions and the characterization of the new compounds ClCF2NHF, CF3CF2NHF, CF3CF2CF2NHF, and CF3CF2CF=NF are presented.

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