2-Bromo-2-(4-fluorophenyl)acetic acid

95%

Reagent Code: #130444
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CAS Number 29270-33-5

science Other reagents with same CAS 29270-33-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.03 g/mol
Formula C₈H₆BrFO₂
badge Registry Numbers
MDL Number MFCD08276759
thermostat Physical Properties
Melting Point 96-100 °C
Boiling Point 288.2±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.725±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in building complex organic compounds. Commonly employed in Friedel-Crafts acylation and esterification reactions to form fluorinated analogs with enhanced metabolic stability. Also utilized in the development of agrochemicals and specialty polymers where fluorine substitution improves performance characteristics.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,880.00
5g
10-20 days ฿14,850.00
2-Bromo-2-(4-fluorophenyl)acetic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in building complex organic compounds. Commonly employed in Friedel-Crafts acylation and esterification reactions to form fluorinated analogs with enhanced metabolic stability. Also utilized in the development of agrochemicals and specialty polymers where fluorine

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in building complex organic compounds. Commonly employed in Friedel-Crafts acylation and esterification reactions to form fluorinated analogs with enhanced metabolic stability. Also utilized in the development of agrochemicals and specialty polymers where fluorine substitution improves performance characteristics.

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