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1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane is a halogenated hydrocarbon with the molecular formula C4H2F6. It is a colorless, volatile liquid with a molecular weight of 184.05 g/mol. 1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane consists of a cyclopropane ring with one difluoromethyl group (-CF2H) and five fluorine atoms. Due to its highly fluorinated structure, it exhibits unique chemical and physical properties, such as high thermal stability, low reactivity, and low toxicity. These characteristics make it a potential candidate for various industrial applications, including refrigerants, fire suppressants, and solvents. However, its environmental impact and potential for ozone depletion should be considered, as it contains multiple fluorine atoms that can contribute to the release of chlorine radicals in the atmosphere.

379-14-6

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379-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 379-14-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 379-14:
(5*3)+(4*7)+(3*9)+(2*1)+(1*4)=76
76 % 10 = 6
So 379-14-6 is a valid CAS Registry Number.

379-14-6Relevant academic research and scientific papers

Cyclopropane Chemistry. Part 4. The Reactions of 1,2,2-Trifluoroethylidene with Alkenes and Pyrolysis of the Resulting Cyclopropanes

Haszeldine, Robert N.,Rowland, Ronald,Speight, James G.,Tipping, Anthony E.

, p. 314 - 324 (2007/10/02)

1,2,2-Trifluoroethylidene, generated by the pyrolysis of (1,1,2,2-tetrafluoroethyl)trifluorosilane, reacts with tetrafluoroethylene, ethylene, and a series of methyl-substituted ethylenes to give the corresponding 1-fluoro-1-difluoromethylcyclopropanes in good yield; cyclohexene gives the corresponding norcarane, and tris(trifluoromethyl)phosphine gives the corresponding phosphorane (CF3)3P(+)-C(-)F-CHF2.Pyrolysis of 1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane affords difluorocarbene and 3H-pentafluoropropene, but pyrolysis of the methyl-substituted cyclopropanes results in the formation of dienes in high yield, e.g. the 1,4-dienes CHF=CF-CMeR-CMe=CH2 from the cyclopropanes (R = H or Me) or 1,3-dienes from the methyl-substituted cyclopropanes, e.g. --> CH2=CMe-C(CHF2)=CH2.In certain cases further dehydrofluorination of the 1,3-dienes affords trienes, e.g. --> CH2=CMe-C(=CHF)-CMe=CH2.

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