Amerigo Scientific
4-Bromoanisole is a useful brominating reagent. It is formed as reaction product in the reaction between HOBr and anisole. Suzuki coupling of 4-bromoanisole with phenylboronic acid catalyzed by palladium pincer complexes has been studied. Heck Reaction of 4-bromoanisole with ethyl acrylates in room-temperature ionic liquids is reported to afford ethyl 4-methoxycinnamate.
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Amerigo Scientific
4-Bromobenzaldehyde diethyl acetal is also known as p-bromobenzaldehyde dimethyl acetal. It is employed during chemical decomposition of pladienolide D to benzylidene acetal.
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Amerigo Scientific
4-Bromobenzaldehyde diethyl acetal is an acetal derivative of 4-bromobenzaldehyde. Its enthalpy of vaporization at boiling point (527. 15K) is 46. 499kjoule/mol. 4-Bromobenzaldehyde diethyl acetal can be synthesized by reacting 4-bromobenzaldehyde with methanol in the presence of triethylamine and titanium chloride.
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Amerigo Scientific
Amerigo Scientific
Electrochemical reduction of 4-bromobenzenediazonium tetrafluoroborate was investigated for the derivatization of the carbon felt (modified carbon surfaces whether glassy carbon or carbon felt).
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Amerigo Scientific
Amerigo Scientific
4-Bromobenzyl alcohol undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls. It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde. It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.
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Amerigo Scientific
4-Bromobenzyl isocyanate (Br-BIC) is an organic building block containing an isocyanate group. Its performance as a polymerizable electrolyte additive to prevent overcharge in lithium ion batteries has been analyzed using various techniques.
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Amerigo Scientific
4-Bromobenzylamine (BBA), also known as p-bromobenzylamine, is an aryl bromide. The selective formation of nitrile or imine from BBA in the presence of red copper has been reported. The formal [4+4] reaction of BBA to form 2,6,9-triazabicyclo[3. 3. 1]nonane derivatives has been investigated.
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