1352721-92-6

Basic information

• Product Name: (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid
• Synonyms: (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid;(S)-1-(2-(tert-Butoxy)-2-oxoethyl)-4-oxopiperidine-2-carboxylic acid
• CAS NO: 1352721-92-6
• Molecular Formula: C12H19NO5
• Molecular Weight: 257.28296
• Mol File: 1352721-92-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 416.6±45.0 °C(Predicted)
• Appearance: /
• Density: 1.205±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 2.16±0.20(Predicted)
• CAS DataBase Reference: (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid(1352721-92-6)
• EPA Substance Registry System: (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid(1352721-92-6)

Safety Data

• Hazardous Substances Data: 1352721-92-6(Hazardous Substances Data)

Usage

Description

(S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid is a complex chemical compound featuring a piperidine ring and a carboxylic acid group. It is widely utilized as a fundamental building block in the realms of organic synthesis and pharmaceutical research. The presence of the tert-butoxycarbonyl (Boc) protecting group ensures the prevention of undesired reactions during the synthesis process. Additionally, the piperidine ring endows the compound with potential biological activity, while the carboxylic acid group facilitates further derivatization and modification. This unique structure and reactivity of (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid render it a promising candidate for applications in drug development and research.

Uses

Used in Pharmaceutical Research:
(S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. The Boc protecting group allows for selective protection of the carboxylic acid during multi-step synthesis, ensuring the successful creation of complex drug molecules.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid serves as a versatile building block for the creation of a wide range of organic compounds. Its piperidine ring and carboxylic acid group provide opportunities for further functionalization and modification, making it a valuable component in the synthesis of various organic molecules.
Used in Drug Development:
(S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid is employed as a crucial component in the development of new drugs. Its potential biological activity, combined with its ability to be further modified and derivatized, makes it an attractive candidate for the development of novel therapeutic agents.
Used in Chemical Research:
In the context of chemical research, (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid is utilized as a model compound to study various chemical reactions and mechanisms. Its complex structure and reactivity provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.
Overall, (S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid is a versatile and valuable compound with a wide range of applications in various industries, including pharmaceutical research, organic synthesis, drug development, and chemical research. Its unique structure and reactivity make it a promising candidate for the development of new drugs and the advancement of scientific knowledge.