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ethyl pentafluorophenyl sulphide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33288-21-0

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33288-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33288-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,8 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33288-21:
(7*3)+(6*3)+(5*2)+(4*8)+(3*8)+(2*2)+(1*1)=110
110 % 10 = 0
So 33288-21-0 is a valid CAS Registry Number.

33288-21-0Downstream Products

33288-21-0Relevant academic research and scientific papers

Synthesis of polyfluoroarylalkyl sulfide compounds

Ward, Wayne E.,Sicree, Stephen,Chen, Brian,Tamborski, Christ

, p. 73 - 78 (2007/10/02)

Syntheses of RC6F4SR' compounds (where R = F, C6H5, H, R' = alkyl, trifluorovinyl) have been accomplished through reaction between ArfSM (where M = Cu, MgX) and an alkyl or trifluorovinyl halide in dimethylacetamide solvent.Minor by-products from competing reactions have been partially characterized by GC-MS analysis. - Keywords: Synthesis; Polyfluoroalkyl sulfides; NMR spectroscopy; Mass spectrometry

Cleavage of pentafluorophenyl-phosphorus and -sulfur bonds by ethylmagnesium bromide

Sicree, Stephen A.,Tamborski, Christ

, p. 269 - 273 (2007/10/02)

Tris(pentafluorophenyl) phosphine and bis (pentafluorophenyl) sulfide react with ethylmagnesium bromide to give products indicating cleavage of the pentafluorophenyl group from phosphorus and sulfur.Ethylated phosphorus and sulfur compounds as well as pentafluorophenylmagnesium bromide are the principal reaction products.Minor products from subsequent reaction the Grignard reagents and cleavage products have also been detected.

SOME REACTIONS OF COPPER(I) PENTAFLUOROTHIOPHENOLATE

Peach, Michael E.,Ritcey, Anna M.

, p. 401 - 406 (2007/10/02)

Copper(I) pentafluorothiophenolate, CuSC6F5 reacted with a number of acyl and alkyl halides in either n-hexane or DMF.The products RCH2SC6F5 ( R = Me, Ph, C6F5S, C6F5SCH2), PH2CHSC6F5, R3CSC6F5 (R = Me, Ph) and RCOSC6F5 (R = Me, C6F5) have been characterized and their spectra, particularly NMR spectra (H-1, C-13, F-19) have been examined.

Partially Fluorinated Heterocyclic Compounds. Part 14. Syntheses of 4,5,6,7-Tetrafluoro-2,3-dihydro-2-methyl-1-benzothiophen and 5,6,7,8-Tetrafluorothiochroman from Pentafluorophenyl Prop-2-enyl Sulphide via the Claisen Rearrangement Intermediate and the

Brooke, Gerald M.,Wallis, Derek I.

, p. 1659 - 1664 (2007/10/02)

Prop-2-enyl 2,3,4,5-tetrafluorophenyl sulphide (1) undergoes a Claisen rearrangement in NN-diethylaniline to give 4,5,6,7-tetrafluoro-2,3-dihydro-2-methyl-1-benzothiophen (4) and 5,6,7,8-tetrafluorothiochroman (5).Pentafluorophenyl prop-2-enyl sulphide (3

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