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Perfluoroisobutenylethylether (PFIBE) is a synthetic chemical compound with the molecular formula C6H2F6O. It is a colorless, odorless, and non-toxic liquid that is insoluble in water. PFIBE is primarily used as a processing aid in the production of fluoropolymers, such as polytetrafluoroethylene (PTFE) and other fluoropolymer resins. It helps to improve the processability and stability of these materials during manufacturing, resulting in enhanced product performance and reduced production costs. Due to its unique properties, PFIBE is also used in various industrial applications, including as a solvent, a surfactant, and a component in fire-fighting foams. However, it is essential to handle PFIBE with care, as it can be harmful if inhaled or ingested, and prolonged exposure may cause adverse health effects.

360-58-7

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360-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 360-58-7 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 360-58:
(5*3)+(4*6)+(3*0)+(2*5)+(1*8)=57
57 % 10 = 7
So 360-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H5F7O/c1-2-14-4(7)3(5(8,9)10)6(11,12)13/h2H2,1H3

360-58-7Relevant academic research and scientific papers

Synthesis of 1-aroyl(1-arylsulfonyl)-4-bis(trifluoromethyl)alkyl semicarbazides as potential physiologically active compounds

Luzina, Elena L.,Popov, Anatoliy V.

, p. 41 - 48 (2013/04/10)

1,1-Bis(trifluoromethyl)alkyl isocyanates obtained from perfluoroisobutene (PFIB) react with aroyl(arylsulfonyl)hydrazines. Twenty eight prospective biologically active polyfluorinated 1,4-substituted semicarbazides were synthesized. The structure of each

Synthesis and anticancer activity of N-bis(trifluoromethyl)alkyl-N′-thiazolyl and N-bis(trifluoromethyl)alkyl-N′-benzothiazolyl ureas

Luzina, Elena L.,Popov, Anatoliy V.

experimental part, p. 4944 - 4953 (2010/02/27)

A number of N-bis(trifluoromethyl)alkyl-N′-thiazolyl and -benzothiazolyl ureas have been synthesized and evaluated for their in vitro antiproliferative activities against the human cancer cell lines at the National Cancer Institute (NCI, USA). The activity was shown for compounds 8a,c and 9a-c. The most sensitive cell lines relative to the tested compounds are: 8c PC-3 (prostate cancer, log GI50 -7.10), 9c SNB-75 (CNS cancer, log GI50 -5.84), 9b UO-31 (renal cancer, log GI50 -5.66), and SR (leukemia, log GI50 -5.44) human cancer cells.

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