6286-82-4

Basic information

• Product Name: 6-Azaspiro[5.5]undecan-6-iuM broMide
• Synonyms: 6-Azaspiro[5.5]undecan-6-iuM broMide;6-Lambda-5-azaspiro[5.5]undecan-6-ylium bromide
• CAS NO: 6286-82-4
• Molecular Formula: Br*C₁₀H₂₀N
• Molecular Weight: 233.16856
• Mol File: 6286-82-4.mol
• Article Data: 6

Chemical Properties

• Melting Point: 310 °C(Solv: isopropanol (67-63-0))
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 6-Azaspiro[5.5]undecan-6-iuM broMide(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Azaspiro[5.5]undecan-6-iuM broMide(6286-82-4)
• EPA Substance Registry System: 6-Azaspiro[5.5]undecan-6-iuM broMide(6286-82-4)

Safety Data

• Hazardous Substances Data: 6286-82-4(Hazardous Substances Data)

Usage

Description

6-Azaspiro[5.5]undecan-6-ium bromide, with the molecular formula C10H20BrN, is a quaternary ammonium salt featuring a positively charged nitrogen atom. This chemical compound is recognized for its utility in various scientific research and industrial applications, particularly in the realms of organic synthesis and pharmaceutical development.

Uses

Used in Organic Synthesis:
6-Azaspiro[5.5]undecan-6-ium bromide is utilized as a catalyst in organic synthesis reactions, where it plays a crucial role in facilitating asymmetric induction and ring-closing reactions. Its effectiveness in these processes is attributed to its unique structural properties and catalytic capabilities.
Used in Pharmaceutical Research and Drug Development:
In the pharmaceutical industry, 6-Azaspiro[5.5]undecan-6-ium bromide is employed as a valuable tool in research and drug development. Its potential applications in the synthesis of new pharmaceutical compounds and the enhancement of existing ones make it a sought-after component in medicinal chemistry.
Used in Antimicrobial Research:
6-Azaspiro[5.5]undecan-6-ium bromide has been studied for its potential antimicrobial properties, indicating its possible use as an agent against various microorganisms. This research avenue could lead to the development of new antimicrobial agents, contributing to the fight against drug-resistant infections.
Overall, 6-Azaspiro[5.5]undecan-6-ium bromide is a versatile compound with applications spanning across chemical synthesis, pharmaceuticals, and antimicrobial research, making it an important asset in scientific and industrial settings.

InChI:InChI=1/C10H20N.BrH/c1-3-7-11(8-4-1)9-5-2-6-10-11;/h1-10H2;1H/q+1;/p-1

Upstream product

• 110-89-4 piperidine 
• 111-24-0 1,5-dibromo-pentane 

Downstream Products

• 110-89-4 piperidine 

Relevant articles and documents

A new polar perovskite coordination network with azaspiroundecane as A-site cation

ABX3 perovskite coordination networks are a rapidly growing sub-class of crystalline coordination networks. At present, synthetic efforts in the field are dominated by the use of commercially available building blocks, leaving the potential for tuning properties via targeted compositional changes largely untouched. Here we apply a rational crystal engineering approach, using 6-azaspiro[5.5]undecane ([ASU]+) as A-site cation for the synthesis of the polar perovskite [ASU][Cd(C2N3)3]. This journal is

METHOD OF PROCESSING CELLULOSIC MATERIALS

The present invention relates to a method of processing cellulosic materials, particularly to a method of dissolving cellulose from cellulose containing feedstock, such as pulp, by contacting the cellulose containing feedstock with thermally and chemically stable ammonium salts, such as spirocyclic ammonium salts or quaternised cyclic ammonium salts. The invention also relates to the use of said ammonium salts for cellulose processing and to a method of manufacturing cellulose- based shaped articles.

Alkaline stability of quaternary ammonium cations for alkaline fuel cell membranes and ionic liquids

The alkaline stability of 26 different quaternary ammonium groups (QA) is investigated for temperatures up to 160°C and NaOH concentrations up to 10 molL-1 with the aim to provide a basis for the selection of functional groups for hydroxide exchange membranes in alkaline fuel cells and of ionic-liquid cations stable in basic conditions. Most QAs exhibit unexpectedly high alkaline stability with the exception of aromatic cations. b-Protons are found to be far less susceptible to nucleophilic attack than previously suggested, whereas the presence of benzyl groups, nearby hetero-atoms, or other electron-withdrawing species promote degradation reactions significantly. Cyclic QAs proved to be exceptionally stable, with the piperidine-based 6-azonia-spiro[5.5]undecane featuring the highest half-life at the chosen conditions. Absolute and relative stabilities presented herein stand in contrast to literature data, the differences being ascribed to solvent effects on degradation.