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Hexafluorodithio-γ-butyrolactone, also known as 1,4-dithiane-1,1,4,4-tetraoxide or 1,4-bis(trifluoromethylsulfonyl)butane-2,3-dione, is a chemical compound with the molecular formula C4F6O4S2. It is a colorless, crystalline solid that is soluble in organic solvents. hexafluorodithio-γ-butyrolactone is characterized by its unique structure, featuring a γ-butyrolactone core with two trifluoromethylsulfonyl groups attached to the carbon atoms at positions 1 and 4. Hexafluorodithio-γ-butyrolactone is primarily used as a reagent in organic synthesis, particularly in the preparation of various sulfur-containing compounds and as a protecting group for alcohols. Due to its stability and reactivity, it has found applications in the pharmaceutical and chemical industries.

1588-28-9

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1588-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1588-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1588-28:
(6*1)+(5*5)+(4*8)+(3*8)+(2*2)+(1*8)=99
99 % 10 = 9
So 1588-28-9 is a valid CAS Registry Number.

1588-28-9Downstream Products

1588-28-9Relevant academic research and scientific papers

Thermal reactions of hexafluorobutadiene and hexafluorocyclobutene with elemental sulphur

Kazmina, N. B.,Mysov, E. I.,Aerov, A. F.,Kagramanova, E. M.

, p. 203 - 208 (1993)

Hexafluorobuta-1,3-diene and hexafluorocyclobutene interact with elemental sulphur under conditions of mutual conversion (>/= 280 deg C) to give the same products, hexafluoro-3,6-dihydro-1,2-dithiine (1), hexafluorothiolene-3 (2) and hexafluorothiolanethione (3).The product composition and ratio depend on the reaction conditions.Dithiine 1 and thiolene 2 were formed in competitive reactions.Their thermal stability and the retrocycloaddition reaction of dithiine 1 have been studied.The latter reaction results in thiolene 2 in addition to the formation of hexafluorocyclobutene.This is consistent with a stepwise mechanism for the retrocycloaddition as well as the cycloaddition reaction.

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