3-(Thiophen-2-yl)benzoic acid

95%

Reagent Code: #240772
fingerprint
CAS Number 29886-63-3

science Other reagents with same CAS 29886-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.25 g/mol
Formula C₁₁H₈O₂S
badge Registry Numbers
MDL Number MFCD03783346
thermostat Physical Properties
Boiling Point 393.6°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of conjugated materials for optoelectronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The thiophene and phenyl groups enable extended π-conjugation, enhancing electron delocalization in functional materials. Also employed in metal-organic frameworks (MOFs) due to its carboxylic acid functionality, which coordinates with metal ions to form porous structures for gas storage or catalysis. Shows potential in medicinal chemistry for developing anti-inflammatory or antimicrobial agents through derivatization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,090.00
inventory 1g
10-20 days ฿5,020.00
3-(Thiophen-2-yl)benzoic acid
No image available

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of conjugated materials for optoelectronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The thiophene and phenyl groups enable extended π-conjugation, enhancing electron delocalization in functional materials. Also employed in metal-organic frameworks (MOFs) due to its carboxylic acid functionality, which coordinates with metal ions

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the preparation of conjugated materials for optoelectronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The thiophene and phenyl groups enable extended π-conjugation, enhancing electron delocalization in functional materials. Also employed in metal-organic frameworks (MOFs) due to its carboxylic acid functionality, which coordinates with metal ions to form porous structures for gas storage or catalysis. Shows potential in medicinal chemistry for developing anti-inflammatory or antimicrobial agents through derivatization.

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...