132182-92-4 | Pentane, 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)-

CAS:132182-92-4 | Pentane, 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)- ,Description

Pentane, 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)-, is a fluorinated hydrocarbon compound that has been studied extensively in recent years due to its unique properties. It is a highly fluorinated compound, with nine fluorine atoms, and has a molecular formula of C6H3F9O2. It has been studied for its potential applications in the fields of chemistry, materials science, and biochemistry. 
 

Scientific Research Applications

Physical Properties and Behavior

Pentane, 1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)-, also referred to as HFE-7300, has been studied for its physical properties, such as liquid density, kinematic viscosity, and surface tension. These properties were observed to vary with temperature, providing valuable information for applications in chemical engineering and materials science (Rausch et al., 2015).

Chemical Reactions

The compound demonstrates interesting behavior in chemical reactions. For example, its room-temperature fluorination with CsSO4F can produce various derivatives, which is relevant in synthetic chemistry and material science (Stavber & Zupan, 1983).

Applications in Organic Chemistry

This compound is utilized in organic chemistry for creating specific molecular structures. For instance, it is used as a connector for photochromic units and fluorophores, contributing to advancements in photophysics and molecular engineering (de Meijere et al., 2007).

In Medical Chemistry

In medicinal chemistry, a bicyclo[1.1.1]pentane, closely related to the queried compound, was integrated into chemical scaffolds to study metabolic stability, highlighting its potential in drug development and pharmacokinetics (Zhuo et al., 2016).

Role in Imaging Techniques

The compound's derivatives, such as (2R*, 3S*)-1-[18F]fluoro-2,3-bis(4-hydroxyphenyl)pentane, have been explored in imaging techniques like positron emission tomography (PET), specifically for targeting estrogen receptors, which can be significant in cancer research (Landvatter et al., 1983).

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