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(E)-3-isopropoxy-3-phenylprop-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14093-56-2

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14093-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14093-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,9 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14093-56:
(7*1)+(6*4)+(5*0)+(4*9)+(3*3)+(2*5)+(1*6)=92
92 % 10 = 2
So 14093-56-2 is a valid CAS Registry Number.

14093-56-2Downstream Products

14093-56-2Relevant academic research and scientific papers

Regioselective and enantioselective iridium-catalyzed allylation of enamines

Weix, Daniel J.,Hartwig, John F.

, p. 7720 - 7721 (2007)

A highly enantioselective and regioselective monoallylation of the enamines of methyl ketones has been developed. After hydrolysis of the enamine (NaOAc/AcOH(aq)), the desiredallylated ketones were obtained in high yields (64-91% isolated yield

Electrochemical properties and reactions of organoboronic acid esters containing unsaturated bonds at their α-position

Ohtsuka, Kazuhiro,Inagi, Shinsuke,Fuchigami, Toshio

, p. G23 - G28 (2017/12/26)

Electrochemical analyses of 2-(cynnamyl)boronic acid pinacol ester and (3-phenyl-2-propynyl)boronic acid pinacol ester, and their trimethylsilyl analogues as well as their parent compounds were comparatively studied by cyclic voltammetry measurements. We

o-benzenedisulfonimide as reusable bronsted acid catalyst for acid-catalyzed organic reactions

Barbero, Margherita,Cadamuro, Silvano,Dughera, Stefano,Venturello, Paolo

, p. 1379 - 1388 (2008/12/21)

Acid-catalyzed organic reactions, such as etherification, esterification, acetal synthesis, cleavage, and interconversion, and pinacol rearrangement were carried out in the presence of catalytic amounts of o-benzenedisulfonimide as Bronsted acid catalyst; the conditions were mild and selective. The catalyst was easily recovered and purified, ready to be used in further reactions, with economic and ecological advantages. Georg Thieme Verlag Stuttgart.

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