4-(2-Bromoethyl)benzoic acid

98.0%

Reagent Code: #143629
label
Alias 2-Fluoro-4-Bromoiodobenzene; 4-Bromo-2-Fluoro-1-Iodine benzene
fingerprint
CAS Number 52062-92-7

science Other reagents with same CAS 52062-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.07 g/mol
Formula C₉H₉BrO₂
badge Registry Numbers
MDL Number MFCD00016541
thermostat Physical Properties
Melting Point 206-208°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized aromatic compounds. Its bromoethyl group allows for further alkylation or coupling reactions, making it valuable in the development of drug candidates targeting central nervous system disorders and anti-inflammatory agents. Commonly employed in the synthesis of esters and amides through activation of the carboxylic acid group. Also utilized in polymer chemistry to introduce aromatic and reactive functionalities into macromolecular structures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿310.00
inventory 1g
10-20 days ฿820.00
inventory 25g
10-20 days ฿15,630.00
inventory 5g
10-20 days ฿3,610.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(2-Bromoethyl)benzoic acid
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized aromatic compounds. Its bromoethyl group allows for further alkylation or coupling reactions, making it valuable in the development of drug candidates targeting central nervous system disorders and anti-inflammatory agents. Commonly employed in the synthesis of esters and amides through activation of the carboxylic acid group. Also utilized in polymer chemistry to introduce aromatic and rea

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized aromatic compounds. Its bromoethyl group allows for further alkylation or coupling reactions, making it valuable in the development of drug candidates targeting central nervous system disorders and anti-inflammatory agents. Commonly employed in the synthesis of esters and amides through activation of the carboxylic acid group. Also utilized in polymer chemistry to introduce aromatic and reactive functionalities into macromolecular structures.

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...