Name: Name:2,5-Thiophenedicarboxylic acid
Brand: AABLOCKS
SKU: AA003FYN
Rating: 90 (10 reviews)

2,5-Thiophenedicarboxylic acid is a versatile chemical compound with diverse applications in coordination chemistry and materials science. Its unique structure, characterized by two carboxylic acid groups attached to a thiophene ring, lends itself to various synthetic pathways and functionalization strategies. One of the primary uses of 2,5-Thiophenedicarboxylic acid is as a thiophene-based linker in the preparation of magnesium coordination networks. This compound serves as a key building block in the construction of coordination polymers and metal-organic frameworks, which exhibit intriguing structural diversity and potential applications in areas such as catalysis, gas storage, and molecular recognition. Furthermore, 2,5-Thiophenedicarboxylic acid serves as a precursor in the synthesis of 2,5-bis-benzoxazoyl-thiophene (EBF), a compound with potential applications in materials science and organic electronics. EBF derivatives are known for their high thermal stability and electron-transporting properties, making them suitable candidates for use in organic semiconductors and optoelectronic devices. Moreover, 2,5-Thiophenedicarboxylic acid finds utility in the synthesis of various coordination polymers and supramolecular assemblies. For example, it is used in the preparation of cobalt(II) thiophenedicarboxylate coordination polymers, which exhibit interesting magnetic and structural properties. Additionally, it is involved in the synthesis of novel mesogenic thiophene-based supramolecular liquid crystals, which have potential applications in display technologies and advanced materials. In summary, 2,5-Thiophenedicarboxylic acid is a versatile compound with applications ranging from coordination chemistry to materials science. Its use as a building block in coordination networks, precursor in the synthesis of functional materials, and key component in the preparation of coordination polymers and liquid crystals highlights its significance in diverse research fields and technological advancements.

Catalog No.: AA003FYN

4282-31-9 | 2,5-Thiophenedicarboxylic acid

Pack Size： 5g

Purity： 97%

in stock

$6.00 $4.00

Pack Size： 10g

Purity： 97%

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$7.00 $5.00

Pack Size： 25g

Purity： 97%

in stock

$10.00 $7.00

Pack Size： 100g

Purity： 97%

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$21.00 $15.00

Pack Size： 500g

Purity： 97%

in stock

$78.00 $55.00

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Technical Information

Catalog Number: AA003FYN

Chemical Name: 2,5-Thiophenedicarboxylic acid

CAS Number: 4282-31-9

Molecular Formula: C6H4O4S

Molecular Weight: 172.1586

MDL Number: MFCD00016896

SMILES: OC(=O)c1ccc(s1)C(=O)O

NSC Number: 81789

Properties

BP: 444.6°C at 760 mmHg

Form: Solid

MP: >300 °C(lit.);

Refractive Index: 1.5500 (estimate)

Storage: Keep in dry area;Room Temperature;

Complexity: 171

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 11

Hydrogen Bond Acceptor Count: 5

Hydrogen Bond Donor Count: 2

Isotope Atom Count: 0

Rotatable Bond Count: 2

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 1.3

Literature fold

Title: Poly[tetra-aqua-bis-(μ(4)-thio-phene-2,5-dicarboxyl-ato)(μ(2)-thio-phene-2,5-dicarboxyl-ato)dieuropium(III)].

Journal: Acta crystallographica. Section E, Structure reports online20120801

Title: Lanthanide-thiophene-2,5-dicarboxylate frameworks: ionothermal synthesis, helical structures, photoluminescent properties, and single-crystal-to-single-crystal guest exchange.

Journal: Inorganic chemistry20120102

Title: Solvothermal synthesis, crystal structure, and properties of lanthanide-organic frameworks based on thiophene-2,5-dicarboxylic acid.

Journal: Dalton transactions (Cambridge, England : 2003)20111121

Title: Poly[bis-(N,N-dimethyl-acetamide)-1κO,2κO-bis-(μ(4)-thio-phene-2,5-di-car-boxyl-ato-1:2:1':2'κO:O:O:O)dizinc].

Journal: Acta crystallographica. Section E, Structure reports online20111101

Title: Influence of halide ions on the chirality and luminescent property of ionothermally synthesized lanthanide-based metal-organic frameworks.

Journal: Chemical communications (Cambridge, England)20110921

Title: Synthesis and optoelectronic properties of symmetrical thiophene based 2,5-disubstiuted 1,3,4-oxadiazoles: highly fluorescent materials for OLED applications.

Journal: Journal of fluorescence20110701

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters20101101

Title: Dimethyl 3,3'-diphenyl-2,2'-[(S)-thio-phene-2,5-diylbis(carbonyl-aza-nedi-yl)]dipropano-ate tetra-hydro-furan monosolvate.

Journal: Acta crystallographica. Section E, Structure reports online20101001

Title: A robust highly interpenetrated metal-organic framework constructed from pentanuclear clusters for selective sorption of gas molecules.

Journal: Inorganic chemistry20100920

Title: Bis(triphenyl-stann-yl) thio-phene-2,5-dicarboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online20090701

Title: A purely lanthanide-based complex exhibiting ferromagnetic coupling and slow magnetic relaxation behavior.

Journal: Inorganic chemistry20090420

Title: 5-tert-Butyl-2-[5-(5-tert-butyl-1,3-benzoxazol-2-yl)-2-thien-yl]-1,3-benzoxazole.

Journal: Acta crystallographica. Section E, Structure reports online20081201

Title: Thermochemistry of 2,5-thiophenedicarboxylic acid.

Journal: The journal of physical chemistry. A20061116

Application fold

2,5-Thiophenedicarboxylic acid is a versatile chemical compound with diverse applications in coordination chemistry and materials science. Its unique structure, characterized by two carboxylic acid groups attached to a thiophene ring, lends itself to various synthetic pathways and functionalization strategies.

One of the primary uses of 2,5-Thiophenedicarboxylic acid is as a thiophene-based linker in the preparation of magnesium coordination networks. This compound serves as a key building block in the construction of coordination polymers and metal-organic frameworks, which exhibit intriguing structural diversity and potential applications in areas such as catalysis, gas storage, and molecular recognition.

Furthermore, 2,5-Thiophenedicarboxylic acid serves as a precursor in the synthesis of 2,5-bis-benzoxazoyl-thiophene (EBF), a compound with potential applications in materials science and organic electronics. EBF derivatives are known for their high thermal stability and electron-transporting properties, making them suitable candidates for use in organic semiconductors and optoelectronic devices.

Moreover, 2,5-Thiophenedicarboxylic acid finds utility in the synthesis of various coordination polymers and supramolecular assemblies. For example, it is used in the preparation of cobalt(II) thiophenedicarboxylate coordination polymers, which exhibit interesting magnetic and structural properties. Additionally, it is involved in the synthesis of novel mesogenic thiophene-based supramolecular liquid crystals, which have potential applications in display technologies and advanced materials.

In summary, 2,5-Thiophenedicarboxylic acid is a versatile compound with applications ranging from coordination chemistry to materials science. Its use as a building block in coordination networks, precursor in the synthesis of functional materials, and key component in the preparation of coordination polymers and liquid crystals highlights its significance in diverse research fields and technological advancements.