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(R)-2-Methylsulfonylamino-2-phenyl-1-methylsulfonyloxyethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

360796-63-0

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360796-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 360796-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,0,7,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 360796-63:
(8*3)+(7*6)+(6*0)+(5*7)+(4*9)+(3*6)+(2*6)+(1*3)=170
170 % 10 = 0
So 360796-63-0 is a valid CAS Registry Number.

360796-63-0Downstream Products

360796-63-0Relevant academic research and scientific papers

Practical Synthesis of Sultams via Sulfonamide Dianion Alkylation: Application to the Synthesis of Chiral Sultams

Lee, Jaemoon,Zhong, Yong-Li,Reamer, Robert A.,Askin, David

, p. 4175 - 4177 (2003)

(Equation presented) A practical synthesis of sultams was developed via intramolecular sulfonamide dianion alkylation. This method has been applied toward the synthesis of chiral sultams, which are synthetically valuable as chiral auxiliaries.

Coordination of (β-N-sulfonylaminoalkyl)phosphines and their analogous arsines to PdII and PtII. Application of the Pd-complexes as chiral catalysts in asymmetric hydrosilylation of 1,3-dienes

Gustafsson,Bergqvist,Frejd

, p. 1452 - 1457 (2007/10/03)

Optically active ligands 2 and 3 were synthesised from phenylglycine and the coordination of ligand 2 to PdCl2(CH3CN)2 and PtCl2(C6H5CN)2 was studied with 1H, 31P and 15N-1H-HMQC NMR spectroscopy. The results indicated P,O rather than P,N bidentate coordination. Both ligands were tested in the palladium catalysed hydrosilylation of cyclic 1,3-dienes. Asymmetric induction of up to 84% (≤25% yield), which is the hitherto highest reported ee value for asymmetric hydrosilylation of 1,3-dienes, was achieved as measured on the allylic alcohols formed after ethanolysis-oxidation of the initially formed allylic silanes.

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