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

95%

Reagent Code: #130444
fingerprint
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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,880.00
inventory 5g
10-20 days ฿14,850.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Bromo-2-(4-fluorophenyl)acetic acid
No image available

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.

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...