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4-phenyl-4-(2-thienyl)-2-butanone is an organic compound with the molecular formula C14H14OS. It is a derivative of 2-butanone, featuring a phenyl group (C6H5) and a 2-thienyl group (C4H3S) attached to the carbonyl carbon. This molecule is characterized by its unique structure, which combines the aromatic properties of the phenyl and thienyl rings with the ketone functional group. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity. The compound is also of interest in materials science for its potential applications in the development of new organic materials.

2691-16-9

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2691-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2691-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,9 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2691-16:
(6*2)+(5*6)+(4*9)+(3*1)+(2*1)+(1*6)=89
89 % 10 = 9
So 2691-16-9 is a valid CAS Registry Number.

2691-16-9Downstream Products

2691-16-9Relevant academic research and scientific papers

Addition of arylboronic acids to arylpropargyl alcohols en route to indenes and quinolines

Panteleev, Jane,Huang, Richard Y.,Lui, Erica K. J.,Lautens, Mark

supporting information; experimental part, p. 5314 - 5317 (2011/12/01)

A regio- and stereoselective rhodium-catalyzed synthesis of trisubstituted allylic alcohols is described. The utility of these synthons is demonstrated in a convenient synthesis of indenes and quinolines.

CHLORO- AND IODOTRIMETHYLSILANE-ACTIVATED ADDITIONS OF ORGANOCOPPER COMPOUNDS TO ENONES AND ENOATES

Bergdahl, Mikael,Lindstedt, Eva-Lotte,Nilsson, Martin,Olsson, Thomas

, p. 2055 - 2062 (2007/10/02)

Organocopper compounds add to enones and enoates in the presence of chloromethylsilane in ether giving the conjugate adducts in preparatively usefu yields via the silyl enol ethers.Presence of lithium iodide is important and excess of chlorotrimethylsilane accelerates the reactions.The combination of organocopper compound, iodotrimethylsilane and dimethyl sulfide gave faster reactions and very high yields, particularly in dichloromethane, where the reaction mixtures gradually became homogeneous.

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