3-(3-Bromophenyl)cyclobutanone

≥95%

Reagent Code: #150621
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CAS Number 885267-15-2

science Other reagents with same CAS 885267-15-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.08 g/mol
Formula C₁₀H₉BrO
badge Registry Numbers
MDL Number MFCD08706340
thermostat Physical Properties
Boiling Point 307.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its cyclic ketone structure with an aryl bromide moiety makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic and heterocyclic systems. Commonly employed in the development of central nervous system agents and anti-inflammatory drugs due to its ability to mimic phenylcyclohexyl scaffolds. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, where the bromine allows for further functionalization and the cyclobutanone provides conformational rigidity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,880.00

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3-(3-Bromophenyl)cyclobutanone
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its cyclic ketone structure with an aryl bromide moiety makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic and heterocyclic systems. Commonly employed in the development of central nervous system agents and anti-inflammatory drugs due to its ability to mimic phenylcyclohexyl scaffolds. Also utilized in medicinal chemistry for structure-activity relationship (SA

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its cyclic ketone structure with an aryl bromide moiety makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic and heterocyclic systems. Commonly employed in the development of central nervous system agents and anti-inflammatory drugs due to its ability to mimic phenylcyclohexyl scaffolds. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, where the bromine allows for further functionalization and the cyclobutanone provides conformational rigidity.

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