1384431-10-0

Basic information

• Product Name: 2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1)
• Synonyms: 2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1);6-(trifluoromethyl)-2-azaspiro[3.3]heptan-6-ol hydrochloride;6-(TRIFLUOROMETHYL)-2-AZASPIRO[3.3]HEPTAN-6-OL HCL
• CAS NO: 1384431-10-0
• Molecular Formula: C7H11ClF3NO
• Molecular Weight: 217.6165496
• Mol File: 1384431-10-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1)(1384431-10-0)
• EPA Substance Registry System: 2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1)(1384431-10-0)

Safety Data

• Hazardous Substances Data: 1384431-10-0(Hazardous Substances Data)

Usage

Description

2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1) is a bicyclic alcohol compound that exists in a hydrochloride salt form. It is characterized by a unique structure and exhibits various biological activities, making it a valuable compound in research and pharmaceutical applications. Its hydrochloride salt form enhances its solubility in water, which is advantageous for use in aqueous solutions. This versatile chemical serves as a chiral auxiliary in organic synthesis and is utilized in the production of pharmaceuticals.

Uses

Used in Research Applications:
2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1) is used as a chiral auxiliary in organic synthesis for its ability to influence the stereochemistry of chemical reactions. This application is crucial for the development of enantiomerically pure compounds, which are essential in various research studies.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, hydrochloride (1:1) is utilized in the development and production of new drugs. Its unique structure and biological activities contribute to the creation of innovative medications, potentially benefiting numerous therapeutic areas.
Used in Aqueous Solutions:
The hydrochloride salt form of 2-Azaspiro[3.3]heptan-6-ol, 6-(trifluoroMethyl)-, increases its solubility in water, making it suitable for use in aqueous solutions. This property is advantageous for applications requiring water-soluble compounds, such as in certain drug formulations or chemical reactions in aqueous media.