3-(3-Bromophenyl)-1,1,1-trifluoropropan-2-one

95%

Reagent Code: #140958
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CAS Number 898787-59-2

science Other reagents with same CAS 898787-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.05 g/mol
Formula C₉H₆BrF₃O
badge Registry Numbers
MDL Number MFCD03844191
thermostat Physical Properties
Boiling Point 247.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.585±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a trifluoromethyl ketone moiety. Its structure allows for selective transformations in organic reactions, making it valuable in constructing complex aromatic and fluorinated compounds. Commonly employed in cross-coupling reactions and nucleophilic additions, it supports the creation of potential drug candidates with enhanced metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,800.00
inventory 1g
10-20 days ฿26,570.00

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3-(3-Bromophenyl)-1,1,1-trifluoropropan-2-one
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a trifluoromethyl ketone moiety. Its structure allows for selective transformations in organic reactions, making it valuable in constructing complex aromatic and fluorinated compounds. Commonly employed in cross-coupling reactions and nucleophilic additions, it supports the creation of potential drug candidates with enhanced metabolic stability and binding

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a trifluoromethyl ketone moiety. Its structure allows for selective transformations in organic reactions, making it valuable in constructing complex aromatic and fluorinated compounds. Commonly employed in cross-coupling reactions and nucleophilic additions, it supports the creation of potential drug candidates with enhanced metabolic stability and binding affinity.

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