5-Bromo-1-naphthoic acid

98%

Reagent Code: #145729
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CAS Number 16726-67-3

science Other reagents with same CAS 16726-67-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.08 g/mol
Formula C₁₁H₇BrO₂
thermostat Physical Properties
Boiling Point 421.2°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of dyes and fluorescent probes due to its aromatic structure and bromine functionality. Its carboxylic acid group allows for easy derivatization, making it valuable in organic synthesis for coupling reactions. Also employed in the preparation of ligands for metal catalysts and in materials science for modifying surface properties. The presence of the bromine atom enables further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, expanding its utility in creating complex organic molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿600.00
5g
10-20 days ฿2,790.00
10g
10-20 days ฿5,340.00
25g
10-20 days ฿12,080.00
100g
10-20 days ฿48,060.00

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5-Bromo-1-naphthoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of dyes and fluorescent probes due to its aromatic structure and bromine functionality. Its carboxylic acid group allows for easy derivatization, making it valuable in organic synthesis for coupling reactions. Also employed in the preparation of ligands for metal catalysts and in materials science for modifying surface properties. The presence of the bromine atom enables further functionalizati

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of dyes and fluorescent probes due to its aromatic structure and bromine functionality. Its carboxylic acid group allows for easy derivatization, making it valuable in organic synthesis for coupling reactions. Also employed in the preparation of ligands for metal catalysts and in materials science for modifying surface properties. The presence of the bromine atom enables further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, expanding its utility in creating complex organic molecules.

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