CAS 1073-31-0

THIOPHENE-3,4-DICARBALDEHYDE

Description:

Thiophene-3,4-dicarbaldehyde is an organic compound characterized by its unique thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features two aldehyde functional groups located at the 3 and 4 positions of the thiophene ring, contributing to its reactivity and potential applications in organic synthesis. It is typically a yellow to brown solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane. The presence of the aldehyde groups makes it a versatile intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Thiophene-3,4-dicarbaldehyde can undergo typical reactions associated with aldehydes, such as oxidation, reduction, and condensation reactions. Its unique structure and functional groups also allow for potential applications in materials science, particularly in the development of conductive polymers and organic electronic devices. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₆H₄O₂S

InChI: InChI=1/C6H4O2S/c7-1-5-3-9-4-6(5)2-8/h1-4H

SMILES: C(=O)c1cscc1C=O

Synonyms:

• 3,4-Thiophenedicarboxaldehyde

3,4-Thiophenedicarboxaldehyde

CAS: 1073-31-0

Formula: C₆H₄O₂S

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 140.16

Ref: 3B-T3343

Thiophene-3,4-dicarbaldehyde

CAS: 1073-31-0

Formula: C₆H₄O₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 140.1598

Ref: IN-DA0084VX

Thiophene-3,4-dicarbaldehyde

CAS: 1073-31-0

Thiophene-3,4-dicarbaldehyde

Purity: 95%

Molecular weight: 140.16g/mol

Ref: 54-OR1050072

Thiophene-3,4-dicarbaldehyde

CAS: 1073-31-0

Purity: 95%

Molecular weight: 140.1600037

Ref: 10-F761269

Thiophene-3,4-dicarbaldehyde

CAS: 1073-31-0

Thiophene-3,4-dicarbaldehyde is an organic solvent that is used in industry. It has been studied for its ability to react with amines and form trichloromethylthioamides. This reaction mechanism is similar to that of thiourea derivatives. Thiophene-3,4-dicarbaldehyde can be used as a ligand for the isolation of macrocyclic compounds. Reaction with amines results in the formation of aliphatic or aromatic amines. Thiophene-3,4-dicarbaldehyde also reacts with dimethylformamide and aromatic amines to form isothiocyanate derivatives.

Formula: C₆H₄O₂S

Purity: Min. 95%

Molecular weight: 140.16 g/mol

Ref: 3D-BAA07331