100012-49-5 | 1,4-Naphthalenedione, 2,3,6,7-tetrabromo-5,8-dihydroxy-

Availability
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Description

• Catalog Number: AA00176
• Chemical Name: 1,4-Naphthalenedione, 2,3,6,7-tetrabromo-5,8-dihydroxy-
• CAS Number: 100012-49-5
• Molecular Formula: C10H2Br4O4
• Molecular Weight: 505.7365
• SMILES: BrC1=C(Br)C(=O)c2c(C1=O)c(O)c(c(c2O)Br)Br

Upstream Synthesis Route

1,4-Naphthalenedione, 2,3,6,7-tetrabromo-5,8-dihydroxy-, commonly referred to as tetrabromonaphthoquinone, is a powerful chemical compound used extensively in chemical synthesis. This compound plays a crucial role in various organic reactions due to its unique structure and properties.In chemical synthesis, tetrabromonaphthoquinone is often employed as a versatile oxidant and electrophilic coupling reagent. Its strong oxidizing properties make it valuable in oxidation reactions, where it facilitates the conversion of various functional groups. Tetrabromonaphthoquinone is particularly efficient in the oxidation of alcohols to carbonyl compounds, highlighting its utility in the preparation of ketones and aldehydes.Furthermore, tetrabromonaphthoquinone is a key component in the synthesis of complex organic molecules, serving as a building block for the construction of diverse chemical structures. Its ability to undergo electrophilic aromatic substitution reactions enables the introduction of functional groups at specific positions on the naphthalene ring, allowing for selective modification of target molecules.Overall, tetrabromonaphthoquinone is a valuable tool in chemical synthesis, offering versatility and efficiency in various synthetic transformations. Its unique reactivity and structural features make it an indispensable reagent for the preparation of sophisticated organic compounds with diverse applications in research and industry.