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

General Description

(S)-1-tert-ButoxycarbonylMethyl-4-oxo-piperidine-2-carboxylic acid is a chemical compound with a complex structure that includes a piperidine ring and a carboxylic acid group. It is commonly used as a building block in organic synthesis and pharmaceutical research. The tert-butoxycarbonyl (Boc) protecting group helps to prevent unwanted reactions during synthesis, while the piperidine ring provides potential biological activity. The carboxylic acid group allows for further derivatization and modification of the compound. Overall, this chemical has potential applications in drug development and research due to its unique structure and reactivity.