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3-(benzylsulfanyl)-1,3-diphenyl-2-propen-1-one is a complex organic compound characterized by its molecular formula C22H20OS. 3-(benzylsulfanyl)-1,3-diphenyl-2-propen-1-one features a 2-propen-1-one (alpha,beta-unsaturated ketone) core, with two phenyl groups attached to the carbonyl carbon (C=O) and a benzylsulfanyl group (benzyl mercaptan) attached to the adjacent carbon. The benzylsulfanyl group consists of a benzyl moiety (C6H5CH2-) and a sulfanyl group (-SH), which together contribute to the compound's unique chemical properties. This molecule is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its structural features.

3920-32-9

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3920-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3920-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,2 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3920-32:
(6*3)+(5*9)+(4*2)+(3*0)+(2*3)+(1*2)=79
79 % 10 = 9
So 3920-32-9 is a valid CAS Registry Number.

3920-32-9Downstream Products

3920-32-9Relevant academic research and scientific papers

Attempted Simmon-Smith reaction on β-alkylthio-α,β- unsaturated ketones: A regiospecific synthesis of 2,4-disubstituted thiophenes

Swaroop, Toreshettahally R.,Roopashree, Rangaswamy,Ila, Hiriyakkanavar,Rangappa, Kanchugarakoppal S.

, p. 147 - 150 (2013/02/21)

A new regiospecific route to 2,4-disubstituted thiophenes has been developed through Simmon-Smith reaction on β-methylthio-α,β- unsaturated ketones. Extension of the reaction to β-ethyl/benzylthio- α,β-unsaturated ketones also gave the corresponding 2,4-disubstituted thiophenes in a regiospecific manner. A probable mechanism involving a carbenoid methylene insertion to divalent sulfur followed by intramolecular aldol condensation has been suggested.

Preparation and reactivity of 1,3-bis(alkylthio)allenes and tetrathiacyclic bisallenes

Shimizu, Toshio,Sakamaki, Kensuke,Miyasaka, Daisuke,Kamigata, Nobumasa

, p. 1721 - 1728 (2007/10/03)

Reactions of Ph2C3 dianion, prepared from 1,3-diphenylpropyne and n- butyllithium, with alkyl thiocyanates or alkane dithiocyanates gave 1,3- bis(alkylthio)allenes 1 or tetrathiacyclic bisallenes 2, respectively. Thermal reactions of 1 gave thiophenes 4 and 7, benzothiepin 5, 1,2- bis(benzylidene)cyclobutane 6, thiete 8, and α,β-unsaturated ketone 9, and the reactions of tetrathiacyclic bisallenes 2a gave a cyclic dimer, 1,2- bis(benzylidene)cyclobutane derivative 10, quantitatively. Irradiation of 1,3-bis(alkylthio)allenes 1 and tetrathiacyclic bisallenes 2a caused rearrangement to give alkynes 18, 20, and 21. In the irradiation of the cyclic bisallenes 2a, isomerizations from dl to meso and meso to dl isomers were also found. In the reactions of allenes 1 and cyclic bisallenes 2a with diphenyl diazomethane, the diazomethane reacted selectively with the double bond rather than with the sulfur atom.

Preparation and thermal reaction of 1,3-bis(alkylthio)allenes

Shimizu, Toshio,Sakamaki, Kensuke,Kamigata, Nobumasa

, p. 8529 - 8532 (2007/10/03)

Reactions of Ph2C3 dianion with alkyl thiocyanates or ethylene 1,2-dithiocyanate give 1,3-bis(alkylthio)allenes or tetrathiacyclic bisallene, respectively. Thermal reactions of 1,3-bis(benzylthio)allene and tetrathiacyclic bisallene afford 2,3,5-triphenylthiophene and 1,2-bismethylidene cyclobutane derivatives, respectively.

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