CAS 31739-56-7

2-(1H-pyrrol-1-yl)benzaldehyde

Description:

2-(1H-pyrrol-1-yl)benzaldehyde, with the CAS number 31739-56-7, is an organic compound characterized by the presence of both a pyrrole and an aldehyde functional group. This compound features a benzaldehyde moiety, where a pyrrole ring is directly attached to the benzene ring at the ortho position relative to the aldehyde group. It typically appears as a yellow to brown liquid or solid, depending on its purity and specific conditions. The compound is known for its aromatic properties and can exhibit interesting reactivity due to the electron-rich nature of the pyrrole ring, which can participate in various chemical reactions, including electrophilic substitutions. Additionally, it may possess biological activity, making it of interest in medicinal chemistry and material science. Its solubility in organic solvents and relatively low solubility in water are typical for compounds of this nature, which can influence its applications in synthesis and research. Safety data should be consulted for handling and storage, as with all chemical substances.

Formula: C₁₁H₉NO

InChI: InChI=1/C11H9NO/c13-9-10-5-1-2-6-11(10)12-7-3-4-8-12/h1-9H

SMILES: c1ccc(c(c1)C=O)n1cccc1

Synonyms:

• benzaldehyde, 2-(1H-pyrrol-1-yl)-
• 2-(1H-PYRROL-1-YL)BENZALDEHYDE

2-(1H-Pyrrol-1-yl)benzaldehyde

CAS: 31739-56-7

Formula: C₁₁H₉NO

Color and Shape: Solid

Molecular weight: 171.1953

Ref: IN-DA00BXK8

2-Pyrrol-1-ylbenzaldehyde

CAS: 31739-56-7

2-Pyrrol-1-ylbenzaldehyde

Formula: C₁₁H₉NO

Purity: 95%

Molecular weight: 171.19526

Ref: 54-OR346713

2-(1H-Pyrrol-1-yl)benzaldehyde

CAS: 31739-56-7

Formula: C₁₁H₉NO

Purity: 95.0%

Molecular weight: 171.199

Ref: 10-F239725

2-Pyrrol-1-ylbenzaldehyde

CAS: 31739-56-7

2-Pyrrol-1-ylbenzaldehyde is a molecule that is transformed to give the corresponding chloride and ketone. The transformation of 2-pyrrol-1-ylbenzaldehyde to the corresponding chloride and ketone is achieved by reaction with diethyl etherate, followed by treatment with acidified hydrochloric acid. This experiment was conducted in order to produce the cyclised compound intramolecularly by sequential halogenation. The synthesis of heterocycles can be achieved through olefination or pyridine ring formation.

Formula: C₁₁H₉NO

Purity: Min. 95%

Molecular weight: 171.2 g/mol

Ref: 3D-GBA73956