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(S)-5-methylpiperidin-2-one is a chiral organic compound with the molecular formula C6H11NO. It is a derivative of piperidin-2-one, featuring a methyl group at the 5-position and a carbonyl group at the 2-position. (S)-5-methylpiperidin-2-one is an important building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. It is widely used in the preparation of chiral amines, which are crucial intermediates in the synthesis of many biologically active molecules. The (S)-enantiomer is particularly valuable due to its potential applications in the development of enantioselective catalysts and chiral ligands.

1192-98-9

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1192-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1192-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1192-98:
(6*1)+(5*1)+(4*9)+(3*2)+(2*9)+(1*8)=79
79 % 10 = 9
So 1192-98-9 is a valid CAS Registry Number.

1192-98-9Upstream product

1192-98-9Relevant academic research and scientific papers

Interrupted Pyridine Hydrogenation: Asymmetric Synthesis of δ-Lactams

Wagener, Tobias,Lückemeier, Lukas,Daniliuc, Constantin G.,Glorius, Frank

, p. 6425 - 6429 (2021)

Metal-catalyzed hydrogenation is an effective method to transform readily available arenes into saturated motifs, however, current hydrogenation strategies are limited to the formation of C?H and N?H bonds. The stepwise addition of hydrogen yields reactive unsaturated intermediates that are rapidly reduced. In contrast, the interruption of complete hydrogenation by further functionalization of unsaturated intermediates offers great potential for increasing chemical complexity in a single reaction step. Overcoming the tenet of full reduction in arene hydrogenation has been seldom demonstrated. In this work we report the synthesis of sought-after, enantioenriched δ-lactams from oxazolidinone-substituted pyridines and water by an interrupted hydrogenation mechanism.

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