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Bromodifluoroacetic acid (BDFA) is a halogenated organic compound that has been widely used in scientific research for its versatility and effectiveness. It has a wide range of applications in biochemistry, physiology, and other scientific fields...
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Bromodifluoroacetic acid (BDFA) is a halogenated organic compound that has been widely used in scientific research for its versatility and effectiveness. It has a wide range of applications in biochemistry, physiology, and other scientific fields.
Bromodifluoroacetic acid derivatives, like Ethyl bromodifluoroacetate (BrCF2COOEt), have been used in copper-catalyzed N-formylation of amines. This process facilitates the smooth formation of N-formamides from a range of primary, secondary, cyclic arylamines, and aliphatic amines (Li et al., 2018).
Chlorodifluoroacetic acid, a close relative of bromodifluoroacetic acid, has shown potential in Reformatskii-type syntheses of fluorine-containing molecules. This offers an attractive extension to the more expensive bromodifluoroacetic acid (Lang & Schaub, 1988).
Ethyl bromodifluoroacetate has been explored for its triple mode of chemical reactivity. It's used as a difluorocarbene precursor for difluoromethylation of soft nucleophiles and shows divergent reactivity based on nucleophilicity and the base used (Polley et al., 2018).
Bromodifluoroacetate is utilized in palladium-catalyzed difluoromethylation of aryl boronic acids. This reaction is significant for drug discovery and development due to its high efficiency and compatibility with various functional groups (Feng et al., 2016).
Bromodifluoroacetate derivatives have been used in the Ugi reaction for preparing difluorinated pseudopeptides, showing the compound's utility in synthesizing complex fluorine-containing molecules (Gouge et al., 2004).
Bromodifluoroacetic acid synthesis technology has been improved through catalytic distillation processes, enhancing the purity and yield of the product (Lupachev et al., 2019).
Phenyl bromodifluoroacetate, a derivative of bromodifluoroacetic acid, has been employed in the Cu-catalyzed deoxytrifluoromethylation of alcohols. This method is useful for medicinal, agricultural, and material chemists (de Azambuja et al., 2019).
Studies on the effect of bromide ion on the distribution of haloacetic acid species in the chlorination and chloramination of waters containing aquatic humic substances have utilized bromodifluoroacetic acid (Cowman & Singer, 1996).
Ethyl bromodifluoroacetate has been used in the Rhodium-catalyzed Reformatsky-type reaction for the synthesis of β-hydroxy-α,α-difluoro carboxylic acid ethyl esters (Sato et al., 2004).
Product Name : | Bromodifluoroaceticacid | ||
CAS No. : | 354-08-5 | Molecular Weight : | 174.93 |
MDL No. : | MFCD02183519 | Purity/ Specification : | |
Molecular Formula : | C2HBrF2O2 | Storage : | Inert atmosphere,2-8°C |
Boiling Point : | - |
GHS Pictogram : | |||
Signal Word : | Danger | Precautionary Statements : | P280-P301+P312-P303+P361+P353-P304+P340-P305+P351+P338-P310 |
UN# : | 1759 | Class : | 8 |
Hazard Statements : | H302-H314 | Packing Group : | Ⅲ |