2-bromo-1-(3-fluorophenyl)ethanone

95%

Reagent Code: #144049
label
Alias 2-Bromo-1-(3-fluorophenyl)ethane-1-one; 3-fluorobromophenone
fingerprint
CAS Number 53631-18-8

science Other reagents with same CAS 53631-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.04 g/mol
Formula C₈H₆BrFO
badge Registry Numbers
MDL Number MFCD00109756
thermostat Physical Properties
Melting Point 34-35 °C
Boiling Point 245.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves as a building block for preparing fluorinated analogs of stimulants and cognition-enhancing agents. Commonly employed in organic synthesis for introducing the 3-fluorophenyl moiety into more complex molecules via nucleophilic substitution or condensation reactions. Its bromo-ketone functionality allows for further derivatization, making it valuable in medicinal chemistry research and the preparation of novel bioactive compounds.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-white to Tan to Light yellow to Yellow to Brown Low-melting Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿400.00
5g
10-20 days ฿1,540.00
25g
10-20 days ฿7,200.00
100g
10-20 days ฿26,620.00
2-bromo-1-(3-fluorophenyl)ethanone
No image available
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves as a building block for preparing fluorinated analogs of stimulants and cognition-enhancing agents. Commonly employed in organic synthesis for introducing the 3-fluorophenyl moiety into more complex molecules via nucleophilic substitution or condensation reactions. Its bromo-ketone functionality allows for further derivatization, making it valuable in medicinal chemistry research and the preparation of novel bioactive compounds.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...