(1-Bromocyclopentyl)(2-chlorophenyl)methanone

95%

Reagent Code: #64714
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CAS Number 6740-86-9

science Other reagents with same CAS 6740-86-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.58 g/mol
Formula C₁₂H₁₂BrClO
badge Registry Numbers
MDL Number MFCD19303925
thermostat Physical Properties
Boiling Point 323.7 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. Its unique structure, featuring both bromine and chlorine substituents, makes it valuable in cross-coupling reactions, which are essential in pharmaceutical and agrochemical research. It can also serve as a building block in the synthesis of biologically active compounds, particularly in the creation of potential drug candidates targeting specific enzymes or receptors. Additionally, its reactivity allows for further functionalization, enabling the production of diverse chemical entities for material science applications.

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Test Parameter Specification
APPEARANCE Yellow to Brown to Dark red to Black Liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿15,471.00

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(1-Bromocyclopentyl)(2-chlorophenyl)methanone
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This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. Its unique structure, featuring both bromine and chlorine substituents, makes it valuable in cross-coupling reactions, which are essential in pharmaceutical and agrochemical research. It can also serve as a building block in the synthesis of biologically active compounds, particularly in the creation of potential drug candidates targeting specific enzymes or receptors. Additionally,

This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. Its unique structure, featuring both bromine and chlorine substituents, makes it valuable in cross-coupling reactions, which are essential in pharmaceutical and agrochemical research. It can also serve as a building block in the synthesis of biologically active compounds, particularly in the creation of potential drug candidates targeting specific enzymes or receptors. Additionally, its reactivity allows for further functionalization, enabling the production of diverse chemical entities for material science applications.

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