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(2S)-tricarbonyl[η-6-(1-diphenylphosphino-2-(p-methoxyphenyl))benzene]chromium(0) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

255841-31-7

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255841-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 255841-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,8,4 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 255841-31:
(8*2)+(7*5)+(6*5)+(5*8)+(4*4)+(3*1)+(2*3)+(1*1)=147
147 % 10 = 7
So 255841-31-7 is a valid CAS Registry Number.

255841-31-7Downstream Products

255841-31-7Relevant academic research and scientific papers

The asymmetric synthesis of phosphorus- and sulfur-containing tricarbonyl(η6-arene)chromium complexes using the chiral base approach

Ariffin, Azhar,Blake, Alexander J.,Ewin, Richard A.,Li, Wan-Sheung,Simpkins, Nigel S.

, p. 3177 - 3189 (2007/10/03)

The use of a simple chiral lithium amide base 2 enables the asymmetric transformation of tricarbonyl-[η6-(diphenylphosphinoyl)benzene]chromium(0) 12 into the corresponding ortho-silylated complex in up to 86% ee. A tin derivative was prepared similarly and was then used to prepare other derivatives via reduction to the corresponding phosphine, followed by transmetallation-electrophilic quench. In the case of tricarbonyl-(η6-1,3-dihydroisobenzothiophene)chromium(0) the chiral base 2 was ineffective, and it was necessary to use a bis-lithium amide base 9 to effect asymmetric substitution in high ee (up to 95%). Decomplexation gave the corresponding chiral sulfides in highly enantiomerically enriched form. In all cases the absolute stereochemistry of the products was derived by conducting X-ray structure determinations on selected examples. The Royal Society of Chemistry 1999.

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