1-(4-Bromophenyl)Cyclopentanecarbonitrile

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Reagent Code: #151117
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CAS Number 143328-19-2

science Other reagents with same CAS 143328-19-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.13 g/mol
Formula C₁₂H₁₂BrN
badge Registry Numbers
MDL Number MFCD01536834
thermostat Physical Properties
Boiling Point 351.3±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.41±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It serves as a building block in the preparation of bioactive molecules due to the presence of both nitrile and aryl groups, which can be further functionalized. The compound is also employed in the production of agrochemicals and specialty organic compounds where a substituted cyclopentane scaffold is required. Its bromo substituent allows for cross-coupling reactions, enabling the construction of more complex molecular architectures in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿850.00
inventory 250mg
10-20 days ฿1,400.00
inventory 1g
10-20 days ฿4,090.00
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1-(4-Bromophenyl)Cyclopentanecarbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It serves as a building block in the preparation of bioactive molecules due to the presence of both nitrile and aryl groups, which can be further functionalized. The compound is also employed in the production of agrochemicals and specialty organic compounds where a substituted cyclopentane scaffold is required. Its bromo substituent allows for cross-coupling reactions,

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It serves as a building block in the preparation of bioactive molecules due to the presence of both nitrile and aryl groups, which can be further functionalized. The compound is also employed in the production of agrochemicals and specialty organic compounds where a substituted cyclopentane scaffold is required. Its bromo substituent allows for cross-coupling reactions, enabling the construction of more complex molecular architectures in medicinal chemistry research.

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