958991-06-5 Usage
Uses
Used in Pharmaceutical Research:
Methyl 6-oxopiperidine-3-carboxylate is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with novel therapeutic properties.
Used in Organic Synthesis:
Methyl 6-oxopiperidine-3-carboxylate serves as a versatile building block in organic synthesis, enabling the creation of a wide range of chemical compounds with diverse applications.
Used in Drug Development:
Due to its functional properties, Methyl 6-oxopiperidine-3-carboxylate is used as a starting material in the development of new drugs and pharmaceuticals. Its potential applications in this field are vast, as it can contribute to the discovery of innovative treatments for various diseases and conditions.
It is crucial to handle Methyl 6-oxopiperidine-3-carboxylate with care and adhere to safety protocols when working with it in laboratory and industrial settings to ensure the safety of personnel and the integrity of the research or production process.
Check Digit Verification of cas no
The CAS Registry Mumber 958991-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,9,9 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 958991-06:
(8*9)+(7*5)+(6*8)+(5*9)+(4*9)+(3*1)+(2*0)+(1*6)=245
245 % 10 = 5
So 958991-06-5 is a valid CAS Registry Number.
958991-06-5Relevant articles and documents
Interrupted Pyridine Hydrogenation: Asymmetric Synthesis of δ-Lactams
Wagener, Tobias,Lückemeier, Lukas,Daniliuc, Constantin G.,Glorius, Frank
, p. 6425 - 6429 (2021/02/22)
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.
