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(R)-1-(1-phenylethylsulfonyl)benzene is a chiral organic compound characterized by its unique molecular structure. It features a benzene ring with a sulfonyl group attached to the 1-position, which is further connected to a 1-phenylethyl group. The "R" configuration indicates that the molecule has a specific three-dimensional arrangement, with the phenylethyl group positioned on the right side when looking at the molecule from the perspective of the sulfur atom. (R)-1-(1-phenylethylsulfonyl)benzene is significant in the field of organic chemistry, particularly in the synthesis of chiral molecules and pharmaceuticals, as the spatial arrangement of atoms can greatly influence the properties and reactivity of the compound. Its applications may extend to the development of drugs, agrochemicals, and other specialty chemicals that require precise stereochemistry for optimal performance.

1601-94-1

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1601-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1601-94-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1601-94:
(6*1)+(5*6)+(4*0)+(3*1)+(2*9)+(1*4)=61
61 % 10 = 1
So 1601-94-1 is a valid CAS Registry Number.

1601-94-1Downstream Products

1601-94-1Relevant academic research and scientific papers

17O NMR Spectra of Tertiary Alcohols, Ethers, Sulfoxides and Sulfones in the Cyclohexyl and 5-Substituted 1,3-Dioxanyl Series and Related Compounds

Manoharan, Muthiah,Eliel, Ernest L.

, p. 225 - 231 (1985)

17O NMR spectra of fifteen cyclohexane-derived tertiary alcohols and related ethers and acetals, six 1,3-dioxane-derived orthoesters, four cyclohexane- and 1,3-dioxane-derived sulfones and the four corresponding sulfoxides, three acyclic sulfones, six alc

Cu2O-catalyzed C–S coupling of quaternary ammonium salts and sodium alkane-/arene-sulfinates

Chen, Hongyi,Huang, Youming,Zeng, Qingle,Zheng, Wenting

, (2020/08/28)

A new protocol for the synthesis of (enantioenriched) benzylic sulfones via the Cu2O-catalyzed C–S bond cross coupling of alkane-/arene-sulfinates and (enantioenriched) benzylic quaternary ammonium salts has been developed. The product benzylic sulfones were obtained in good to high yields (75–96%). Chiral arylmethyl sulfones with high enantiomeric excess (90–94% ee) were also synthesized in the presence of Cu2O and 1,1′-bis-(diphenylphosphino)ferrocene (dppf).

Conversion of Amines into Phenylsulfides and Phenylselenides via Ditosylamides

Mller, Paul,Thi, Minh Phuong Nguyen

, p. 2168 - 2172 (2007/10/02)

Amines are converted in good to excellent yields to phenylsulfides or phenylselenides via nucleophilic displacement on the corresponding ditosylamides.The conversion of (-)-(S)-1-phenylethylamine to the chiral phenylsulfide 6 was found to proceed with inv

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