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1-Phenyl-1-(p-chlorphenyl)-propen is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97379-32-3

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97379-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97379-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,7 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 97379-32:
(7*9)+(6*7)+(5*3)+(4*7)+(3*9)+(2*3)+(1*2)=183
183 % 10 = 3
So 97379-32-3 is a valid CAS Registry Number.

97379-32-3Relevant academic research and scientific papers

Friedel-Crafts alkenylation of arenes using alkynes catalysed by metal trifluoromethanesulfonates

Tsuchimoto,Maeda,Shirakawa,Kawakami

, p. 1573 - 1574 (2000)

Metal trifluoromethanesulfonates [M(OTf)(n); M = Sc, Zr, In] catalyse the Friedel-Crafts alkenylation of arenes using alkynes, including internal alkynes, to give, through an alkenyl cation intermediate, 1,1-diarylalkenes in high to excellent yields.

Copper-Catalyzed Hydroarylation of Internal Alkynes: Highly Regio- and Diastereoselective Synthesis of 1,1-Diaryl, Trisubstituted Olefins

Kortman, Gregory D.,Hull, Kami L.

, p. 6220 - 6224 (2017/09/15)

The copper-catalyzed hydroarylation of internal, unsymmeric alkynes is presented. Trisubstituted alkenes are obtained as single diastereomers in good to excellent yields and excellent regioselectivities. The scope of the reaction is presented with respect to alkyne and aryl iodide coupling partners. Initial mechanistic experiments indicate a hydrocupration event followed by a two-electron oxidative addition/reductive elimination pathway.

Synthesis and in Vitro Pharmacology of Arpromidine and Related Phenyl(pyridylalkyl)guanidines, a Potential New Class of Positive Inotropic Drugs

Buschauer, Armin

, p. 1963 - 1970 (2007/10/02)

Replacement of the cimetidine moiety in impromidine (1, N1--N2-thio>ethyl>guanidine) by more lipophilic H2-nonspecific pheniramine-like structures resulted

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