Cart (0)
No products in the cart.
Purchase CAS:21379-33-9,view related peer-reviewed papers,technical documents,similar products,MSDS & more.
4,4,4-Trifluoro-3-(trifluoromethyl)butane-1,3-diol (TFB-1,3-diol) is an organic compound with a variety of uses in different scientific fields. It is an alcohol with a molecular weight of 250.19 g/mol and a boiling point of 55.5 °C. It is a colorless liquid with a pungent odor and is soluble in water. TFB-1,3-diol has ...
4,4,4-Trifluoro-3-(trifluoromethyl)butane-1,3-diol (TFB-1,3-diol) is an organic compound with a variety of uses in different scientific fields. It is an alcohol with a molecular weight of 250.19 g/mol and a boiling point of 55.5 °C. It is a colorless liquid with a pungent odor and is soluble in water. TFB-1,3-diol has been used in a variety of applications, including as a reagent in organic synthesis, a solvent in the production of pharmaceuticals, and a reactant in the synthesis of other organic compounds. In addition, it has been studied for its biochemical and physiological effects, and its potential applications in lab experiments.
4,4,4-Trifluoro-3-(trifluoromethyl)butane-1,3-diol is utilized in the synthesis of aryl-substituted β-diketonato-ruthenium(II)-polypyridyl sensitizers for dye-sensitized solar cells. These complexes exhibit intense visible light absorption, which is crucial for solar cell applications (Islam et al., 2006).
The compound contributes to the formation of hydrogen-bonded structures in certain trifluoromethylated alcohols. This is evident in studies involving X-ray crystal structures of related compounds (Singh, Twamley, & Shreeve, 2001).
It plays a role in polycondensations involving aliphatic dicarboxylic acids and aliphatic diols. The presence of this compound aids in achieving higher molecular weights in the resulting polyesters (Buzin, Lahcini, Schwarz, & Kricheldorf, 2008).
This chemical is used in synthesizing trifluoromethyl-containing heterocycles, which are important in various chemical reactions (Song et al., 2008).
It is instrumental in synthesizing novel trifluoromethylated β-acetal-diols, which have applications in further chemical syntheses (Zanatta, Rosa, Loro, Bonacorso, & Martins, 2001).
The compound is used in microwave-assisted synthesis processes to create fused heterocycles incorporating the trifluoromethyl moiety (Shaaban, 2008).
It's used in synthesizing ytterbium(III) beta-diketonate complexes, which are important for studying luminescence in chemistry (Martín‐Ramos et al., 2013) .
This compound forms complexes with nickel(II) and copper(II), which are significant in the study of metal-organic chemistry (Woods et al., 2009).
It's involved in the formation of unexpected trifluoromethyl-containing bridged heterocycles, an area of interest in organic synthesis (Jiang & Zhu, 2008).
Product Name : | 4,4,4-Trifluoro-3-(trifluoromethyl)butane-1,3-diol | ||
CAS No. : | 21379-33-9 | Molecular Weight : | 212.09 |
MDL No. : | MFCD15143412 | Purity/ Specification : | |
Molecular Formula : | C5H6F6O2 | Storage : | - |
Boiling Point : | - |
GHS Pictogram : | |||
Signal Word : | Precautionary Statements : | ||
UN# : | - | Class : | - |
Hazard Statements : | - | Packing Group : | - |