Zinc bromide - ≥99.9% metals basis, used for Zinc bromide can be used as:
A catalyst to synthesize β-hydroxy ketones by stereoselective semipinacol rearrangement of α-hydroxy epoxides.
A safe brominating source for the oxidative bromination of alkenes and
Zinc bromide - ≥99.9% metals basis, used for Zinc bromide can be used as:
A catalyst to synthesize β-hydroxy ketones by stereoselective semipinacol rearrangement of α-hydroxy epoxides.
A safe brominating source for the oxidative bromination of alkenes and
≥99.9% metals basis for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 130 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht
Zinc bromide is an inorganic salt. Zinc bromide supported on hydroxyapatite (Zn-HAP) promotes the synthesis of 3-substituted indoles. Zinc bromide (ZnBr2) may be used for the following studies: Removal of dimethoxytrityl ethers from deoxynucleosides. Removal of N-acyl protecting group in nucleoside derivatives. Alkylation of O-silylated dienolates of unsaturated ketones and esters. As catalyst in the synthesis of α-perfluoroalkylated homoallylic alcohols.
Zinc bromide can be used as:
A catalyst to synthesize β-hydroxy ketones by stereoselective semipinacol rearrangement of α-hydroxy epoxides.
A safe brominating source for the oxidative bromination of alkenes and alkynes in combination with lead tetraacetat
This compound belongs to the class of inorganic compounds known as transition metal bromides. These are inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom a transition metal.
External Descriptors
Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
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