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2-((R)-Toluene-4-sulfinyl)-pentan-3-one is a chiral organic compound characterized by its unique structure and properties. It features a pentan-3-one backbone, which is a five-carbon ketone, with the ketone group located at the third carbon. The compound is further distinguished by the presence of a (R)-toluen-4-sulfinyl group attached to the second carbon. This sulfinyl group is derived from toluene, a benzene derivative, and is crucial for the compound's stereochemistry. The (R)-configuration indicates that the sulfur atom is attached to the larger group (in this case, the toluene ring) in a specific three-dimensional arrangement. 2-((R)-Toluene-4-sulfinyl)-pentan-3-one is of interest in organic chemistry, particularly in the synthesis of chiral molecules and as a potential intermediate in the production of pharmaceuticals and other specialty chemicals. Its specific reactivity, solubility, and other physical properties are influenced by the presence of the sulfinyl group and the chiral center, making it a valuable compound for research and industrial applications.

56146-61-3

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56146-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56146-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,4 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56146-61:
(7*5)+(6*6)+(5*1)+(4*4)+(3*6)+(2*6)+(1*1)=123
123 % 10 = 3
So 56146-61-3 is a valid CAS Registry Number.

56146-61-3Downstream Products

56146-61-3Relevant academic research and scientific papers

Chiral α-Sulphinyl Hydrazones as Effective Reagents for Stereoselective Aldol-type Condensation

Annunziata, Rita,Cozzi, Franco,Cinquini, Mauro,Colombo, Lino,Gennari, Cesare,et al.

, p. 251 - 254 (2007/10/02)

The stereoselective aldol-type synthesis of optically active β-hydroxy hydrazones and β-hydroxy ketones mediated by chiral α-sulphinyl hydrazones is described.In some cases a good degree of enantioselectivity (up to 88percent) is achieved.The factors affe

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