2,5-Thiophenedicarboxylic acid

98%

Reagent Code: #239758
label
Alias thiophene-2,5-dicarboxylic acid; 2,5-thiophene dicarboxylic acid, OB acid
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CAS Number 4282-31-9

science Other reagents with same CAS 4282-31-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.16 g/mol
Formula C₆H₄O₄S
badge Registry Numbers
EC Number 224-284-2
MDL Number MFCD00016896
thermostat Physical Properties
Melting Point >300 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a building block in the synthesis of coordination polymers and metal-organic frameworks (MOFs) due to its ability to chelate metal ions through carboxylate groups. Its rigid aromatic structure contributes to the formation of thermally stable and porous materials, which are explored for gas storage, catalysis, and sensing applications. Also employed in the development of functional polymers and organic electronics, where the thiophene core enhances electronic properties. Additionally, it serves as a precursor in the preparation of specialty chemicals and pharmaceuticals requiring heterocyclic scaffolds.

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Test Parameter Specification
Purity (GC) 98-100%
Appearance White to off-white powder or crystals
Infrared Spectrum CONFORMS TO STRUCTURE
Melting Point (°C) >300°C

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿720.00
inventory 500g
10-20 days ฿5,380.00
inventory 100g
10-20 days ฿1,380.00

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2,5-Thiophenedicarboxylic acid
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Used as a building block in the synthesis of coordination polymers and metal-organic frameworks (MOFs) due to its ability to chelate metal ions through carboxylate groups. Its rigid aromatic structure contributes to the formation of thermally stable and porous materials, which are explored for gas storage, catalysis, and sensing applications. Also employed in the development of functional polymers and organic electronics, where the thiophene core enhances electronic properties. Additionally, it serves as

Used as a building block in the synthesis of coordination polymers and metal-organic frameworks (MOFs) due to its ability to chelate metal ions through carboxylate groups. Its rigid aromatic structure contributes to the formation of thermally stable and porous materials, which are explored for gas storage, catalysis, and sensing applications. Also employed in the development of functional polymers and organic electronics, where the thiophene core enhances electronic properties. Additionally, it serves as a precursor in the preparation of specialty chemicals and pharmaceuticals requiring heterocyclic scaffolds.

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