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Hexafluor-1,2-bis-2-phenylmercapto-cyclopenten is a complex organic compound with the molecular formula C18H12F6S2. It is characterized by a cyclopenten ring structure, which is a five-membered carbon ring, with two phenylmercapto groups (C6H5SH) attached to the 1 and 2 positions. These phenylmercapto groups are further modified by the presence of six fluorine atoms, which are distributed across the molecule. Hexafluor-1,2-bis-2-phenylmercapto-cyclopenten is of interest in organic chemistry and materials science due to its unique structure and potential applications in the synthesis of fluorinated compounds and as a precursor in the development of new materials with specific properties.

745-18-6

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745-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 745-18-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,4 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 745-18:
(5*7)+(4*4)+(3*5)+(2*1)+(1*8)=76
76 % 10 = 6
So 745-18-6 is a valid CAS Registry Number.

745-18-6Downstream Products

745-18-6Relevant academic research and scientific papers

Fluoroalkene chemistry. Part 2. Reactions of thiols with some toxic 1,2-dichlorinated polyfluorocycloalkenes

Timperley, Christopher M.

, p. 1265 - 1272 (2004)

1,2-Dichlorotetrafluorocyclobutene, 1,2-dichlorohexafluorocyclopentene and 1,2-dichlorooctafluorocyclohexene were treated with an equimolar amount of benzenethiol, 2-methoxybenzenethiol, 3-methoxybenzenethiol and 4-methoxybenzenethiol in acetonitrile with potassium carbonate. Each combination of fluoroalkene and thiol gave a mixture of mono and bis vinyl substitution products whose proportions depended on the ring size of the fluorocycloalkene and the size and electronic characteristics of the thiol. Treatment of 1,2-dichlorotetrafluorocyclobutene with one or two molar equivalents of N -acetylcysteine isopropyl ester in acetonitrile with potassium carbonate produced the mono and bis vinyl substitution products accordingly. The results support the contention that the high inhalation toxicity of the fluorocycloalkenes is due to reaction with two molar equivalents of biological thiols in the lung.

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