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(RS,S,S,RS)-2,4-bis(phenylsulfinyl)pentane is a chiral organic compound characterized by its unique molecular structure. It consists of a pentane backbone with two phenylsulfinyl groups attached to the 2nd and 4th carbon atoms. The compound exhibits a specific stereochemistry, with the RS configuration at both ends of the molecule, and the S configuration at the central carbon. This arrangement of chiral centers results in distinct spatial arrangements of the phenyl groups, which can have implications for its physical and chemical properties, such as reactivity and interactions with other chiral molecules. The compound's structure and stereochemistry make it a potential candidate for applications in asymmetric synthesis and as a chiral auxiliary in organic chemistry.

88243-86-1

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88243-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88243-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,4 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88243-86:
(7*8)+(6*8)+(5*2)+(4*4)+(3*3)+(2*8)+(1*6)=161
161 % 10 = 1
So 88243-86-1 is a valid CAS Registry Number.

88243-86-1Downstream Products

88243-86-1Relevant academic research and scientific papers

Oligomerization of Vinyl Monomers. 17. Stereoselective Methylation of 1-Lithio-1,3-bis(phenylsulfinyl)butane. Kinetic vs. Thermodynamic Control in the Formation of Diastereomeric Ion Paors

Buese, Mark A.,Hogen-Esch, Thieo E.

, p. 4509 - 4513 (2007/10/02)

The addition of (R) or (R,S)-vinyl phenyl sulfoxide (3) to (R)- or (R,S)-1-lithio-(phenylsulfinyl)ethane (2) was carried out in THF at -78 deg C, and the adduct anion 4 was protonated or methylated to produce 1,3-bis(phenylsulfinyl)butane (6) or 2,4-bis(p

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