7-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL

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Reagent Code: #51336
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CAS Number 1196049-18-9

science Other reagents with same CAS 1196049-18-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.07 g/mol
Formula C₉H₉BrO
thermostat Physical Properties
Boiling Point 292.0±35.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.617±0.06 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as a key building block for the development of more complex chemical structures. Its bromine atom makes it a versatile building block for various coupling reactions, such as Suzuki or Heck reactions, which are essential in the synthesis of pharmaceuticals and agrochemicals. Additionally, the presence of the hydroxyl group allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Researchers often employ it in the study of drug discovery, particularly in the design of molecules targeting central nervous system disorders due to its structural similarity to certain bioactive compounds. Its application extends to material science, where it can be used to synthesize novel organic materials with specific electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,473.00
inventory 1g
10-20 days ฿33,651.00
inventory 100mg
10-20 days ฿8,478.00

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7-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL
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This compound is primarily utilized in organic synthesis as a key building block for the development of more complex chemical structures. Its bromine atom makes it a versatile building block for various coupling reactions, such as Suzuki or Heck reactions, which are essential in the synthesis of pharmaceuticals and agrochemicals. Additionally, the presence of the hydroxyl group allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Researche

This compound is primarily utilized in organic synthesis as a key building block for the development of more complex chemical structures. Its bromine atom makes it a versatile building block for various coupling reactions, such as Suzuki or Heck reactions, which are essential in the synthesis of pharmaceuticals and agrochemicals. Additionally, the presence of the hydroxyl group allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Researchers often employ it in the study of drug discovery, particularly in the design of molecules targeting central nervous system disorders due to its structural similarity to certain bioactive compounds. Its application extends to material science, where it can be used to synthesize novel organic materials with specific electronic or optical properties.

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