118334-96-6

Basic information

• Product Name: 1,1,2,2,3,3,4,4,4-Nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester
• Synonyms: 1,1,2,2,3,3,4,4,4-Nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester;1,1,1,3,3,3-Hexafluoropropan-2-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
• CAS NO: 118334-96-6
• Molecular Formula: C₇HF₁₅O₃S
• Molecular Weight: 450.122088
• Mol File: 118334-96-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 46.5-47.5 °C(Press: 30 Torr)
• Appearance: /
• Density: 1.773±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,1,2,2,3,3,4,4,4-Nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2,2,3,3,4,4,4-Nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester(118334-96-6)
• EPA Substance Registry System: 1,1,2,2,3,3,4,4,4-Nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester(118334-96-6)

Safety Data

• Hazardous Substances Data: 118334-96-6(Hazardous Substances Data)

Usage

Description

1,1,2,2,3,3,4,4,4-nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester is a complex organic compound characterized by its unique molecular structure with multiple fluorine and trifluoromethyl groups. 1,1,2,2,3,3,4,4,4-nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester is known for its reactivity and stability, making it a valuable component in various chemical processes and applications.

Uses

Used in Organic Synthesis:
1,1,2,2,3,3,4,4,4-nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester is used as a reactant in organic synthesis for its ability to participate in a range of chemical reactions. Its fluorinated nature allows it to be a versatile building block for creating new molecules with specific properties, such as enhanced solubility, stability, or reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,1,2,2,3,3,4,4,4-nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester is used as an intermediate in the development of new drugs. Its unique properties can be exploited to design drugs with improved pharmacokinetics, such as better absorption, distribution, metabolism, and excretion profiles.
Used in Chemical Research:
1,1,2,2,3,3,4,4,4-nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester is also utilized in chemical research as a model system to study the effects of fluorination on molecular properties and reactivity. It can provide insights into the behavior of fluorinated molecules and contribute to the advancement of fluoroorganic chemistry.
Used in Material Science:
In material science, 1,1,2,2,3,3,4,4,4-nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester can be employed in the development of novel materials with specific characteristics, such as enhanced chemical resistance, thermal stability, or non-stick properties.
Overall, the diverse applications of 1,1,2,2,3,3,4,4,4-nonafluoro-butane-1-sulfonic acid 2,2,2-trifluoro-1-trifluoromethyl-ethyl ester demonstrate its potential as a valuable compound in various scientific and industrial fields.

Upstream product

• 375-72-4 Nonafluorobutanesulfonyl fluoride 
• 920-66-1 1,1,1,3',3',3'-hexafluoro-propanol 

Downstream Products

• 4141-91-7 1,1,1,3,3,3-Hexafluoroisopropyl iodide 
• 431-87-8 2-chloro-1,1,1,3,3,3-hexafluoropropane 

Relevant articles and documents

AQUEOUS METHODS FOR MAKING FLUORINATED SULFONATE ESTERS

Methods of making a fluorinated sulfonate ester include combining a perfluoroalkanesulfonyl halide and a fluorinated alcohol in water in the presence of hydroxide ion, and recovering at least a portion of the resultant fluorinated sulfonate ester.