7-BROMOBICYCLO[2.2.1]HEPTANE

97%

Reagent Code: #149443
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CAS Number 13237-88-2

science Other reagents with same CAS 13237-88-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.07 g/mol
Formula C₇H₁₁Br
badge Registry Numbers
MDL Number MFCD00674502
thermostat Physical Properties
Boiling Point 75 °C20 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.38 g/mL at 20 °C(lit.)
Storage Room temperature, dry, sealed

description Product Description

Used primarily as a synthetic intermediate in organic chemistry, this compound serves in the construction of complex bicyclic frameworks found in pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions, enabling the introduction of various substituents to the norbornane structure. It is also employed in the development of novel ligands and catalysts due to the rigidity of its bridged ring system. Additionally, it finds use in medicinal chemistry for probing steric and electronic effects in drug design.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,770.00
inventory 1g
10-20 days ฿38,520.00
inventory 5g
10-20 days ฿167,150.00

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7-BROMOBICYCLO[2.2.1]HEPTANE
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Used primarily as a synthetic intermediate in organic chemistry, this compound serves in the construction of complex bicyclic frameworks found in pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions, enabling the introduction of various substituents to the norbornane structure. It is also employed in the development of novel ligands and catalysts due to the rigidity of its bridged ring system. Additionally, it finds use in medicinal chemistry for probing steric

Used primarily as a synthetic intermediate in organic chemistry, this compound serves in the construction of complex bicyclic frameworks found in pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions, enabling the introduction of various substituents to the norbornane structure. It is also employed in the development of novel ligands and catalysts due to the rigidity of its bridged ring system. Additionally, it finds use in medicinal chemistry for probing steric and electronic effects in drug design.

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