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Bis(hexafluoroisopropyl)disulfide, also known as 1,1'-(Sulfanediylbis(1,1,2,2-tetrafluoro-2-(trifluoromethyl)ethane-2,2-diyl))bis(trifluoromethane), is a chemical compound with the molecular formula C6F14S2. It is a colorless liquid with a pungent odor and is used as a reagent in organic synthesis, particularly in the preparation of various sulfur-containing compounds. The compound is characterized by its high thermal stability and low reactivity, making it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.

1540-07-4

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1540-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1540-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1540-07:
(6*1)+(5*5)+(4*4)+(3*0)+(2*0)+(1*7)=54
54 % 10 = 4
So 1540-07-4 is a valid CAS Registry Number.

1540-07-4Downstream Products

1540-07-4Relevant academic research and scientific papers

Reaction of fluoroolefins with sulfur chlorides in hydrogen fluoride-boron trifluoride system

Petrov, Viacheslav A.

, p. 325 - 327 (2001)

The reaction of tetrafluoroethylene (1), perfluorovinyl ether (3), hexafluoropropene (5), and 2-H-pentafluoropropene (7) with sulfur chlorides in anhydrous HF/BF3 system has been studied. The reaction with S2Cl2 at 40-100°C produces a mixture of the corresponding di- and trisulfides along with smaller amounts of sulfenyl- and thiosulfenyl chlorides. In case of 7 the use of BF3 catalyst results higher yields and selectivity of the process under milder conditions. The reaction of 5 and SCl2 in HF/BF3 at 100°C is selective, gives (CF3)2CFSCl, isolated in 65% yield.

New Syntheses of Trifluoromethyl-Substituted Heterocycles

Rabe, Gerd,Sundermeyer, Joerg,Roesky, Herbert W.,Schmidt, Hans-Georg,Noltemeyer, Mathias

, p. 691 - 696 (2007/10/02)

Dimeric hexafluorothioacetone (HFTA) (1) reacts with thiourea or phenylthiourea to give 1,2,4-dithiazolines 2a and 2b.Similarly, 1,2,4-thiaselenazoline 3 is obtained from the reaction of 1 with selenourea.Reaction of 1 with oxamic hydrazide or thiosemicarbazide leads to acyclic molecules 4 and 5.Besides 5, the cyclic isomer 6 is also observed in solution.The N-trifluoroacetyl derivative 6a is obtained from the reaction of 5 with trifluoroacetic anhydride.The structures of 2b, 3, 5 and 6a have been determined by single-crystal X-ray crystallography.

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