2,3-Dibromonorbornadiene

≥95%(GC)

Reagent Code: #180137
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CAS Number 128780-28-9

science Other reagents with same CAS 128780-28-9

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Weight 249.93 g/mol
Formula C₇H₆Br₂
inventory_2 Storage & Handling
Storage Room temperature

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Used primarily in organic synthesis as a versatile building block for complex cyclic compounds. Its strained norbornadiene framework with reactive bromine atoms makes it valuable in cross-coupling reactions, particularly in palladium-catalyzed transformations to form carbon-carbon bonds. Commonly employed in the development of pharmaceuticals, agrochemicals, and specialty materials where rigid, polycyclic scaffolds are needed. Also utilized in research settings to prepare functionalized hydrocarbons and advanced intermediates in total synthesis. The presence of two bromine atoms allows for sequential functionalization, enabling precise control over molecular architecture.

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10-20 days ฿4,860.00

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2,3-Dibromonorbornadiene
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Used primarily in organic synthesis as a versatile building block for complex cyclic compounds. Its strained norbornadiene framework with reactive bromine atoms makes it valuable in cross-coupling reactions, particularly in palladium-catalyzed transformations to form carbon-carbon bonds. Commonly employed in the development of pharmaceuticals, agrochemicals, and specialty materials where rigid, polycyclic scaffolds are needed. Also utilized in research settings to prepare functionalized hydrocarbons and

Used primarily in organic synthesis as a versatile building block for complex cyclic compounds. Its strained norbornadiene framework with reactive bromine atoms makes it valuable in cross-coupling reactions, particularly in palladium-catalyzed transformations to form carbon-carbon bonds. Commonly employed in the development of pharmaceuticals, agrochemicals, and specialty materials where rigid, polycyclic scaffolds are needed. Also utilized in research settings to prepare functionalized hydrocarbons and advanced intermediates in total synthesis. The presence of two bromine atoms allows for sequential functionalization, enabling precise control over molecular architecture.

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