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1,2-Pentanedione, 3,3,4,4,5,5,5-heptafluoro-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69481-44-3

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69481-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69481-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,8 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69481-44:
(7*6)+(6*9)+(5*4)+(4*8)+(3*1)+(2*4)+(1*4)=163
163 % 10 = 3
So 69481-44-3 is a valid CAS Registry Number.

69481-44-3Downstream Products

69481-44-3Relevant academic research and scientific papers

FLUORO-KETONES VI. SYNTHESIS OF PERFLUORO DI- AND TETRA-KETONES FROM 1,1-DICHLOROBENZYLLITHIUM AND PERFLUOROESTERS

Chen, Loomis S.,Tamborski, Christ

, p. 269 - 280 (2007/10/02)

The reaction of C6H5CCl2Li with perfluorinated mono and diesters yields fluorochloroketones in high yield.Hydrolysis of such compounds produces alpha-beta fluorinated di- and tetra-ketones, respectively.Various hydrates of the fluorinated ketones have bee

SYNTHESIS OF FLUORINATED α-DIKETONES AND SOME INTERMEDIATES

Hudlicky, M.

, p. 383 - 406 (2007/10/02)

Reactions of perfluoroalkylcopper compounds with α-ketoacyl chlorides were used for the synthesis of fluorinated α-diketones.Heptafluoropropylcopper prepared from copper bronze and 1-iodoheptafluoropropane reacted with benzoylformyl chloride to give heptafluoro-1-phenyl-1,2-pentanedione, with trimethylpyruvyl chloride to give 2,2-dimethyl-5,5,6,6,7,7,7-heptafluoro-3,4-heptanedione, and with 3,3,4,4,5,5,5-heptafluoro-2-keto-pentanoyl chloride or oxalyl chloride to give tetradecafluoro-4,5-octane-dione.Syntheses of fluorinated acetylenes, cyanohydrins, α-hydroxy acids, α-keto acids, their chlorides, and other intermediates for the syntheses of α-diketones by the above route and by other methods are described.An interesting seven-membered ring containing β-hydroxy ketone was obtained by an intramolecular aldol condensation of a fluorinated bis(methyl) ketone.

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