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Benzonitrile, 3-(3-oxobutyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30780-22-4

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30780-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30780-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,8 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30780-22:
(7*3)+(6*0)+(5*7)+(4*8)+(3*0)+(2*2)+(1*2)=94
94 % 10 = 4
So 30780-22-4 is a valid CAS Registry Number.

30780-22-4Downstream Products

30780-22-4Relevant academic research and scientific papers

Direct cobalt-catalyzed conjugate addition of functionalized aryl halides and triflates: A new strategy for the conjugate addition onto methyl vinyl ketone

Amatore, Muriel,Gosmini, Corinne

, p. 1073 - 1076 (2009)

An efficient cobalt-catalyzed method for the direct conjugate addition of functionalized aryl halides or triflates onto methyl vinyl ketone is described. The experimentally simple procedure relies on the use of a catalytic system consisting of CoBr2(Bpy) and zinc and does not require the preformation of a stoichiometric organometallic species. The approach described herein displays considerable functional-group compatibility at good to excellent yields. Georg Thieme Verlag Stuttgart.

Nickel-catalyzed electrochemical arylation of activated olefins

Condon, Sylvie,Dupre, Daniel,Falgayrac, Gilles,Nedelec, Jean-Yves

, p. 105 - 111 (2007/10/03)

Nickel-catalyzed electrochemical conjugate additions of substituted aryl bromides to activated olefins under recently optimized reaction conditions are reported. Good to high yields were obtained, whatever the nature of substituents in the meta- and para-positions of the benzene ring. In the ortho-substituted series, yields were good with electron-donating substituents, but low with electron-withdrawing groups. The activation of aryl chlorides and the sequential functionalization of aryl dihalides were also investigated.

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