CAS 498-62-4

3-Thiophenecarboxaldehyde

Description:

3-Thiophenecarboxaldehyde, also known as 3-thiophenecarbaldehyde, is an organic compound characterized by a thiophene ring substituted with a formyl group at the 3-position. Its molecular formula is C6H5OS, indicating the presence of a sulfur atom within the five-membered aromatic ring. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. 3-Thiophenecarboxaldehyde is known for its reactivity, particularly in electrophilic aromatic substitution reactions, and can participate in various chemical transformations, including condensation and addition reactions. It is used in organic synthesis, particularly in the preparation of thiophene derivatives and as an intermediate in the production of pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this compound, as it may be harmful if inhaled or absorbed through the skin.

Formula: C₅H₄OS

InChI: InChI=1S/C5H4OS/c6-3-5-1-2-7-4-5/h1-4H

InChI key: InChIKey=RBIGKSZIQCTIJF-UHFFFAOYSA-N

SMILES: C(=O)C=1C=CSC1

Synonyms:

• 3-Formylthiophene
• 3-Thenaldehyde
• 3-Thienaldehyde
• 3-Thienophenecarboxyaldehyde
• 3-Thienylcarboxaldehyde
• 3-Thiophenaldehyde
• 3-Thiophene Carboxyaldehyde
• 3-Thiophenealdehyde
• 3-Thiophenecarbaldehyde
• Nsc 172858
• Thiofuran-3-carboxaldehyde
• Thiophen-3-Carboxaldehyde
• Thiophen-3-aldehyde
• Thiophen-3-carbaldehyd
• Thiophene-3-carbaldehyde
• Thiophene-3-carboxaldehyde
• Tiofeno-3-Carbaldehido
• 3-Thiophenecarboxaldehyde

3-Thiophenecarboxaldehyde

CAS: 498-62-4

Formula: C₅H₄OS

Purity: >98.0%(GC)

Color and Shape: Colorless to Brown clear liquid

Molecular weight: 112.15

Ref: 3B-T0864

Thiophene-3-carboxaldehyde, 96%

CAS: 498-62-4

Thiophene-3-carboxaldehyde has been used in the synthesis of series of 4-substituted 2-thiophenesulfonamides, acetal and ketal derivatives of 4?-demethylepipodophyllotoxin--D-glucoside and epipodophyllotoxin--D-glucoside. Also has been used to produce 1,2-di-3-thienyl-2-hydroxyethanone (3,3?-thenoin

Formula: C₅H₄OS

Purity: 96%

Color and Shape: Liquid, Clear colorless to yellow to dark brown

Molecular weight: 112.15

Ref: 02-A14628

3-Thiophenecarboxaldehyde

CAS: 498-62-4

Formula: C₅H₄OS

Purity: 97%

Color and Shape: Liquid

Molecular weight: 112.1497

Ref: IN-DA0033S9

Thiophene-3-carboxaldehyde

CAS: 498-62-4

Thiophene-3-carboxaldehyde

Formula: C₅H₄OS

Purity: 97%

Color and Shape: black liquid

Molecular weight: 112.14966g/mol

Ref: 54-OR5054

Thiophene-3-carboxaldehyde

CAS: 498-62-4

Formula: C₅H₄OS

Molecular weight: 112.15

Ref: 7W-GK8187

Thiophene-3-carboxaldehyde

CAS: 498-62-4

Formula: C₅H₄OS

Purity: 97%

Color and Shape: Liquid

Molecular weight: 112.15

Ref: 10-F045073

Thiophene-3-carboxaldehyde

CAS: 498-62-4

Thiophene-3-carboxaldehyde is an electron-rich, reactive chemical substance that can be used as a polymer film. It is a heterocyclic compound with a thiophene ring and a carbonyl group in the 3-position. Thiophene-3-carboxaldehyde is synthesized by reacting methyl ketones with glycol ethers. This reaction produces redox potential, malonic acid, and nmr spectra.

Formula: C₅H₄OS

Purity: Min. 95%

Color and Shape: Colorless Clear Liquid

Molecular weight: 112.15 g/mol

Ref: 3D-FT11818

3-Thiophenecarboxaldehyde

Controlled Product

CAS: 498-62-4

Formula: C₅H₄OS

Color and Shape: Neat

Molecular weight: 112.15

Ref: TR-T344845