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(E)-1-dimethylamino-2-phenylsulfonylethylene is an organic compound with the molecular formula C10H13NO2S. It is a conjugated diene, featuring a double bond between the dimethylamino group and the phenylsulfonyl group. This molecule is characterized by its electron-rich nature due to the presence of the dimethylamino group, which can participate in various chemical reactions, such as Diels-Alder reactions, due to its ability to act as a nucleophile. The phenylsulfonyl group provides stability to the molecule and can also engage in reactions, such as nucleophilic aromatic substitution. (E)-1-dimethylamino-2-phenylsulfonylethylene is of interest in organic synthesis and may have potential applications in the development of pharmaceuticals and other specialty chemicals.

74858-07-4

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74858-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74858-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,5 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74858-07:
(7*7)+(6*4)+(5*8)+(4*5)+(3*8)+(2*0)+(1*7)=164
164 % 10 = 4
So 74858-07-4 is a valid CAS Registry Number.

74858-07-4Downstream Products

74858-07-4Relevant academic research and scientific papers

An efficient preparation of β-dimethylaminovinyl sulfone and sulfoximide, and investigation of their reactivity as dipolarophiles

Pesa, Nela,Welch, Chris J.,Boa, Andrew N.

, p. 599 - 607 (2005)

A simple reaction affording (E)-1-dimethylamino-2-phenylsulfonylethylene, and S-((E)-2-(N′N′-dimethylamino)ethenyl)-5-phenyl-N-(p- tolylsulfonyl) sulfoximide in high yields is described. A reversal in regioselectivity was observed when the ss-dimethylamin

Reaction of 1-Lithio-1-arylthio(or alkylthio)methyltrimethylsilane with Acid Derivatives. A Novel Synthesis of Functionalized Vinyl Sulfides

Agawa, Toshio,Ishikawa, Minori,Komatsu, Mitsuo,Ohshiro, Yoshiki

, p. 1205 - 1208 (2007/10/02)

Reactions of 1-lithio-1-phenylthiomethyl- (1a) and 1-lithio-1-methylthiomethyltrimethylsilane (1b) with amides, an ester, acid anhydrides, a urea, and a carbonate are described which provide useful routes to functionalized vinyl sulfides.The reaction of 1 with amides gave β-functionalized vinyl sulfides, 1-dialkylamino-2-phenylthio (or methylthio)ethylenes, in 40-95percent yields and the reaction could be extended to the sulfonyl derivatives of 1 to afford 1-dialkylamino-2-phenylsulfonyl(or methylsulfonyl)ethylenes.Although ethyl benzoate and some acid anhydrides were not good substrates for this reaction, tetramethylurea and diethyl carbonate gave α-functionalized vinyl sulfides, 1-amidovinyl- and 1-(ethoxycarbonyl)vinyl sulfides, in moderate yields when treated with 1a followed by addition of benzaldehyde.

REACTION OF PHENOXYVINYL SULFONES WITH AMINES

Vasil'eva, M. A.,Bychkova, T. I.,Kalabina, A. V.,Dobrynina, L. M.

, p. 1249 - 1251 (2007/10/02)

The reaction of phenoxyvinyl sulfones with strongly basic aliphatic amines and hydrazines takes place with substitution of the phenoxy group.As a result of the reaction trans-dialkylaminovinyl sulfones and β-phenylsulfonylacetaldehyde hydrazones are obtai

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