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4-methyl-benzenesulfinic acid 2-cyclohexen-1-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

690232-46-3

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690232-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 690232-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,2,3 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 690232-46:
(8*6)+(7*9)+(6*0)+(5*2)+(4*3)+(3*2)+(2*4)+(1*6)=153
153 % 10 = 3
So 690232-46-3 is a valid CAS Registry Number.

690232-46-3Relevant academic research and scientific papers

Synthesis and Chemistry of a New P-N Chelating Ligand; (R) and (S)-6-(2'-Diphenylphosphino-1'-naphthyl)phenanthridine

Valk, Jean-Marc,Claridge, Timothy D. W.,Brown, John M.,Hibbs, David,Hursthouse, Michael B.

, p. 2597 - 2610 (1995)

A synthesis of the title phosphinamine (PHENAP) is described, following previously established methodology.Resolution via the C,N-palladocycle derived from (R)-N,N-dimethyl-α-methyl-1-naphthylamine led to two crystallographically defined complexes with the (R,S)-form posessing a chelated ligand and the (R,R)-form open with only the phosphine coordinated.Palladium allyl complexes of the ligand were strikingly different from those of the corresponding isoquinoline ligand QUINAP, and the differences could be rationalised by recourse to molecular models, with the additional fused arene ring of PHENAP playing a critical part in defining the coordination sphere through its steric pressure.A brief appraisal of Pd-catalysed allylic alkylation reactions was performed with the new ligand.

Palladium-Catalyzed Enantioselective 1,3-Rearrangement of Racemic Allylic Sulfinates: Asymmetric Synthesis of Allylic Sulfones and Kinetic Resolution of an Allylic Sulfinate

Jagusch, Thomas,Gais, Hans-Joachim,Bondarev, Oleg

, p. 2731 - 2736 (2007/10/03)

Described is an asymmetric synthesis of cyclic and acyclic allylic S-aryl. and S-alkyl sulfones through a highly selective palladium(0)-catalyzed 1,3-rearrangement of racemic allylic sulfinates. Treatment of racemic cyclic and acyclic allylic S-tolyl- and

Rearrangement of Some Allylic Sulphinate Esters to Allylic Sulphones. Ion-pair and Sigmatropic Shift Mechanisms

Knight, Derek J.,Whitham, Gordon H.,Williams, Jonathan G.

, p. 2149 - 2152 (2007/10/02)

The mechanism of rearrangement of a number of allylic sulphinate esters to the corresponding allylic sulphones on heating in formamide has been investigated as a function of substrate structure.Simple systems such as crotyl and α-methylallyl-sulphinate ap

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