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Propane, 2-diazo-1,1,1,3,3,3-hexafluoro-, also known as hexafluoropropylene diazide or HFPD, is a chemical compound with the molecular formula C3F6N2. It is a colorless, highly reactive gas that is used as a precursor in the synthesis of various fluoropolymers, such as polyvinylidene fluoride (PVDF) and polytetrafluoroethylene (PTFE). HFPD is produced through the reaction of hexafluoropropylene with sodium azide, and it is known for its high reactivity and potential use in the production of fluorinated compounds with unique properties, such as improved thermal stability and chemical resistance. Due to its hazardous nature and potential for explosive decomposition, HFPD requires careful handling and storage under controlled conditions.

684-23-1

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684-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 684-23-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 684-23:
(5*6)+(4*8)+(3*4)+(2*2)+(1*3)=81
81 % 10 = 1
So 684-23-1 is a valid CAS Registry Number.

684-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-diazo-1,1,1,3,3,3-hexafluoropropane

1.2 Other means of identification

Product number -
Other names Propane,2-diazo-1,1,1,3,3,3-hexafluoro

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:684-23-1 SDS

684-23-1Relevant academic research and scientific papers

Polyfluorinated Organic Compounds. X. Reaction of Perfluoro(2-methyl-2-pentene) with Sodium Azide

Zhuzhgov,Furin

, p. 710 - 714 (2007/10/03)

Perfluoro(2-methyl-2-pentene) reacts with sodium azide in acetonitrile at -10°C to yield perluoro-(3-azido-2-methyl-2-pentene), which is stable only at low temperature. When the reaction is carried out in the presence of ethanol at the same temperature, stable 5-ethoxy-5-pentafluoroethyl-4,4-bis(trifluorornemyl)-4,5-dihydro-1H-1,2,3- triazole is formed. The reaction in the system acetonitrile-ethanol at 2°C yields ethyl pentafluoropropanimidate and bis(trifluoromethyl)diazomethane. Thermolysis and photolysis of perfluoro-(3-azido-2-methyl-2-pentene) in CCl4, as well as in C6H6, toluene, or pentane, results in fromation of 3-pentafluoroethyl-2,2-bis(trifluoromethyl)-2H-azirine.

PERFLUOROALKYL DERIVATIVES OF NITROGEN. PART LIII. REACTION OF PERFLUORO(2,5-DIMETHYL-4-OXA-3,5-DIAZAHEX-2-ENE) WITH FLUORO-OLEFINS

Fisher, R.,Haszeldine, R. N.,Tipping, A. E.

, p. 155 - 164 (2007/10/02)

Thermal decomposition of the title compound at 140 deg C gives mainly nitrogen, hexafluoroacetone and tetrakistrifluoromethylhydrazine while reaction with tetrafluoroethylene and chlorotrifluoroethylene affords equimolar mixtures of the 1:1 adducts (CF3)2C=NCF2CFXON(CF3)2 and (CF3)2C=NOCFXCF2N(CF3)2 (X=F and Cl) in highly yield via four-centre addition or a radical-cage process.

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