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1,1,1,4,4,4-hexafluoro-2,3-bis(trifluoromethyl)but-2-ene is a complex organic compound with the molecular formula C6F12. It is characterized by the presence of six fluorine atoms and two trifluoromethyl groups attached to a butene backbone. This molecule exhibits a unique structure, with the fluorine atoms and trifluoromethyl groups distributed across the carbon chain, resulting in a highly fluorinated and electronegative molecule. Due to its chemical properties, it has potential applications in various fields, such as the production of specialty chemicals, pharmaceuticals, and materials science. The compound's stability, reactivity, and unique electronic properties make it an interesting subject for further research and development in the field of fluorochemistry.

360-57-6

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360-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 360-57-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 360-57:
(5*3)+(4*6)+(3*0)+(2*5)+(1*7)=56
56 % 10 = 6
So 360-57-6 is a valid CAS Registry Number.

360-57-6Relevant academic research and scientific papers

Bis(trifluoromethyl)sulfine, (CF3)2C=SO: New Syntheses and Some Reactions

Elsaesser, Andreas,Sundermeyer, Wolfgang

, p. 4553 - 4560 (2007/10/02)

New methods for the synthesis of bis(trifluoromethyl)sulfine (sulfoxide) (9) are reported.Pyrolysis, photolysis, and hydrolysis of the compound were investigated as well as the typical behaviour in reactions with the thiocarbonyl group (thiophosgene), with anthracene (Diels-Alder addition) and halogens.

Synthesis and Properties of Tetrakis(trifluoromethyl)-1,3-dithietane S-Oxides and Bis(trifluoromethyl)sulfine

Elsaesser, Andreas,Sundermeyer, Wolfgang,Stephenson, David S.

, p. 116 - 123 (2007/10/02)

The corresponding S-oxides 2-6 could be obtained by oxidation of 2,2,4,4-tetrakis(trifluoromethyl)-1,3-dithietane (1).Similar oxidation of 2,2,4,4-tetrakis(trifluoromethyl)thiirane (8) yields the episulfoxide 12, but not the episulfone 14.Pyrolysis of 2, 3, 5, and 6 have been investigated and bis(trifluoromethyl)sulfine (7) could be isolated as the first member of perfluoroalkylsulfines as well as the sulfonylfluoride 13 being the product of isomerization of bis(trifluoromethyl)sulfene (9). 7 could also be obtained by ring opening from 3 with bases and by oxidation of hexafluorothioacetone (11), respectively.Solvolytic ring opening in 5 and 6 yields the sulfones 16 and 17.

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