5-Bromo-4-methylthiophene-2-carboxylic acid

98%

Reagent Code: #153404
fingerprint
CAS Number 54796-53-1

science Other reagents with same CAS 54796-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.0717 g/mol
Formula C₆H₅BrO₂S
badge Registry Numbers
MDL Number MFCD11110671
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that contain thiophene scaffolds. Its functional groups enable coupling reactions and derivatization, making it valuable in medicinal chemistry for constructing heterocyclic compounds with potential antimicrobial, anti-inflammatory, or anticancer activity. Also employed in materials science for designing organic semiconductors and conjugated polymers due to the electron-rich nature of the thiophene ring. The bromine atom allows for palladium-catalyzed cross-coupling reactions, facilitating the introduction of complex substituents in advanced synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,220.00
inventory 5g
10-20 days ฿7,800.00
inventory 25g
10-20 days ฿33,880.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-4-methylthiophene-2-carboxylic acid
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that contain thiophene scaffolds. Its functional groups enable coupling reactions and derivatization, making it valuable in medicinal chemistry for constructing heterocyclic compounds with potential antimicrobial, anti-inflammatory, or anticancer activity. Also employed in materials science for designing organic semiconductors and conjugated polymers due to the electron

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that contain thiophene scaffolds. Its functional groups enable coupling reactions and derivatization, making it valuable in medicinal chemistry for constructing heterocyclic compounds with potential antimicrobial, anti-inflammatory, or anticancer activity. Also employed in materials science for designing organic semiconductors and conjugated polymers due to the electron-rich nature of the thiophene ring. The bromine atom allows for palladium-catalyzed cross-coupling reactions, facilitating the introduction of complex substituents in advanced synthetic pathways.

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...