1331825-48-9

Basic information

• Product Name: 1-Boc-3-allyl-3-hydroxypiperidine
• Synonyms: 1-Boc-3-allyl-3-hydroxypiperidine;tert-butyl 3-hydroxy-3-(prop-2-en-1-yl)piperidine-1-carboxylate;tert-Butyl 3-allyl-3-hydroxypiperidine-1-carboxylate
• CAS NO: 1331825-48-9
• Molecular Formula: C13H23NO3
• Molecular Weight: 241.32662
• Mol File: 1331825-48-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 318.1±35.0 °C(Predicted)
• Appearance: /
• Density: 1.052±0.06 g/cm3(Predicted)
• PKA: 14.60±0.20(Predicted)
• CAS DataBase Reference: 1-Boc-3-allyl-3-hydroxypiperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Boc-3-allyl-3-hydroxypiperidine(1331825-48-9)
• EPA Substance Registry System: 1-Boc-3-allyl-3-hydroxypiperidine(1331825-48-9)

Safety Data

• RIDADR: UN2811
• Hazardous Substances Data: 1331825-48-9(Hazardous Substances Data)

Usage

Description

1-Boc-3-allyl-3-hydroxypiperidine is a chemical compound with the formula C14H25NO3. It is an allyl-substituted piperidine derivative featuring a tert-butoxycarbonyl (Boc) protecting group on the nitrogen atom. 1-Boc-3-allyl-3-hydroxypiperidine is recognized for its unique structural features, making it a significant molecule in the realm of organic chemistry and drug discovery.

Uses

Used in Organic Synthesis:
1-Boc-3-allyl-3-hydroxypiperidine is utilized as a chiral building block for the preparation of various pharmaceuticals and biologically active molecules. Its hydroxyl group and allyl substituent contribute to its versatility as an intermediate in the synthesis of complex organic molecules.
Used in Drug Development:
In the pharmaceutical industry, 1-Boc-3-allyl-3-hydroxypiperidine is employed as a key intermediate in the development of new drugs. Its unique structural attributes facilitate the creation of novel therapeutic agents with potential applications in treating various diseases and conditions.
Used in Medicinal Chemistry Research:
1-Boc-3-allyl-3-hydroxypiperidine is also used in medicinal chemistry research to explore its potential as a precursor for the synthesis of compounds with specific biological activities. This research aids in advancing the understanding of molecular interactions and the development of more effective and targeted therapies.