CAS 10035-16-2

1-Benzofuran-5-carbaldehyde

Description:

1-Benzofuran-5-carbaldehyde, with the CAS number 10035-16-2, is an organic compound characterized by a benzofuran moiety with an aldehyde functional group at the 5-position. This compound typically appears as a pale yellow to light brown liquid or solid, depending on its purity and specific conditions. It is known for its aromatic properties, which contribute to its potential applications in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The presence of the aldehyde group makes it reactive, particularly in condensation reactions and nucleophilic additions. Additionally, 1-benzofuran-5-carbaldehyde may exhibit biological activity, making it of interest in medicinal chemistry. Its solubility in organic solvents and limited solubility in water are typical for compounds of this nature, influencing its handling and application in laboratory settings. Safety precautions should be observed when working with this compound, as with many organic chemicals, due to potential irritant properties.

Formula: C₉H₆O₂

InChI: InChI=1/C9H6O2/c10-6-7-1-2-9-8(5-7)3-4-11-9/h1-6H

SMILES: c1cc2c(cco2)cc1C=O

Benzofuran-5-carbaldehyde

CAS: 10035-16-2

Formula: C₉H₆O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 146.1427

Ref: IN-DA0001PK

Benzo[b]furan-5-carboxaldehyde

CAS: 10035-16-2

Benzo[b]furan-5-carboxaldehyde

Formula: C₉H₆O₂

Purity: 98%

Color and Shape: light yellow crystalline low melting solid

Molecular weight: 146.14g/mol

Ref: 54-OR10877

1-Benzofuran-5-carbaldehyde

CAS: 10035-16-2

Formula: C₉H₆O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 146.145

Ref: 10-F034059

1-Benzofuran-5-carbaldehyde

CAS: 10035-16-2

1-Benzofuran-5-carbaldehyde is a synthetic compound that inhibits the enzyme ido1. It has been shown to have potent cytotoxicity, potent inhibition, and neurotrophic properties in a number of cell lines. 1-Benzofuran-5-carbaldehyde also exhibits inhibitory effects on the enzymes hydrolyzing dopamine, which is involved in the synthesis of norepinephrine and epinephrine. The chemical structure of 1-benzofuran-5-carbaldehyde closely resembles that of dopamine and its derivatives, and can be used for the treatment of neurodegenerative diseases such as Parkinson's disease.

Formula: C₉H₆O₂

Purity: Min. 95%

Color and Shape: Yellow To Brown Solid

Molecular weight: 146.14 g/mol

Ref: 3D-FB10743