CAS 99902-03-1

2-thiophen-3-ylbenzaldehyde

Description:

2-Thiophen-3-ylbenzaldehyde, with the CAS number 99902-03-1, is an organic compound characterized by the presence of both a thiophene ring and a benzaldehyde functional group. This compound features a thiophene moiety substituted at the 3-position with a benzaldehyde group, which contributes to its aromatic properties. It typically appears as a yellow to brown liquid or solid, depending on its purity and specific conditions. The presence of the thiophene ring imparts unique electronic properties, making it of interest in various applications, including organic synthesis and materials science. The compound is likely to exhibit moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic aromatic structure. Additionally, it may participate in various chemical reactions, such as electrophilic substitutions or condensation reactions, due to the reactivity of the aldehyde group. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₁₁H₈OS

InChI: InChI=1/C11H8OS/c12-7-9-3-1-2-4-11(9)10-5-6-13-8-10/h1-8H

SMILES: c1ccc(c(c1)C=O)c1ccsc1

Synonyms:

• 2-(3-Thienyl)benzaldehyde
• Benzaldehyde, 2-(3-thienyl)-

2-(Thiophen-3-yl)benzaldehyde

CAS: 99902-03-1

Formula: C₁₁H₈OS

Purity: %

Color and Shape: Liquid

Molecular weight: 188.2456

Ref: IN-DA003VUU

2-(Thien-3-yl)benzaldehyde

CAS: 99902-03-1

2-(Thien-3-yl)benzaldehyde

Purity: 95%

Molecular weight: 188.25g/mol

Ref: 54-OR7590

2-Thiophen-3-yl-benzaldehyde

CAS: 99902-03-1

Formula: C₁₁H₈OS

Purity: 95+%

Molecular weight: 188.24

Ref: 10-F032232

2-Thiophen-3-yl-benzaldehyde

CAS: 99902-03-1

2-Thiophen-3-yl-benzaldehyde is a research chemical with various potential applications. It has been studied for its antibiotic properties, specifically as a ribosome-inactivating agent. Additionally, it has shown interactions with glutamate and muscarinic receptors, suggesting potential therapeutic effects in neurological disorders. This compound has also demonstrated antinociceptive properties, indicating its potential as an analgesic. Furthermore, 2-Thiophen-3-yl-benzaldehyde has been investigated as an inhibitor of thymidylate synthase, an enzyme involved in DNA synthesis. Its ability to interact with saponins and nuclear components further highlights its versatility for research purposes.

Formula: C₁₁H₈OS

Purity: Min. 95%

Molecular weight: 188.24 g/mol

Ref: 3D-ZDA90203