1241726-10-2

Basic information

• Product Name: (S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate
• Synonyms: (S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate
• CAS NO: 1241726-10-2
• Molecular Formula: C10H18N2O3
• Molecular Weight: 214.26152
• Mol File: 1241726-10-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 354.3±35.0 °C(Predicted)
• Appearance: /
• Density: 1.135±0.06 g/cm3(Predicted)
• PKA: 7.79±0.20(Predicted)
• CAS DataBase Reference: (S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate(1241726-10-2)
• EPA Substance Registry System: (S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate(1241726-10-2)

Safety Data

• Hazardous Substances Data: 1241726-10-2(Hazardous Substances Data)

Usage

Description

(S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate, a compound with the molecular formula C10H18N2O3, is a derivative of the amino acid proline. It is characterized by its unique structure and properties, which make it a valuable chiral building block in organic synthesis. This chemical is widely recognized for its role in pharmaceutical research and drug development, where it serves as a key intermediate in the production of various medicinal compounds. Its significance in the field of medicinal chemistry and drug discovery is substantial due to its ability to contribute to the creation of a broad spectrum of pharmaceutical products.

Uses

Used in Pharmaceutical Research and Drug Development:
(S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate is used as a chiral building block in the pharmaceutical industry for its ability to facilitate the synthesis of a wide range of medicinal compounds. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate is utilized as a key intermediate. Its incorporation into the drug development process aids in the design and synthesis of novel pharmaceutical products, potentially leading to breakthroughs in the treatment of various diseases and conditions.
Used in Organic Synthesis:
(S)-tert-butyl 3-aMino-2-oxopiperidine-1-carboxylate is also used as a valuable chiral building block in organic synthesis, where it contributes to the creation of complex molecular structures with specific stereochemistry. This application is crucial for the development of enantiomerically pure compounds, which are essential in various chemical and pharmaceutical processes.