CAS 39856-98-9

Benzo[b]thiophene-3-carboxaldehyde, 2-bromo-

Description:

Benzo[b]thiophene-3-carboxaldehyde, 2-bromo- is an organic compound characterized by its structure, which includes a benzo[b]thiophene core substituted with a carboxaldehyde group and a bromine atom. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including stability and reactivity due to the presence of the aldehyde functional group. The bromine substitution can influence its reactivity, making it a potential candidate for various chemical reactions, such as electrophilic aromatic substitution or nucleophilic addition. The presence of the thiophene ring contributes to its electronic properties, potentially enhancing its utility in organic synthesis and materials science. Additionally, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry. As with many organic compounds, the specific physical properties, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which the compound is studied. Overall, Benzo[b]thiophene-3-carboxaldehyde, 2-bromo- represents a versatile structure in organic chemistry with potential applications in various fields.

Formula: C₉H₅BrOS

2-Bromobenzo[b]thiophene-3-carbaldehyde

CAS: 39856-98-9

Formula: C₉H₅BrOS

Color and Shape: Solid

Molecular weight: 241.1044

Ref: IN-DA0076W0

2-Bromobenzo[b]thiophene-3-carbaldehyde

CAS: 39856-98-9

Formula: C₉H₅BrOS

Purity: 95.0%

Molecular weight: 241.1

Ref: 10-F454498

2-Bromobenzo[b]thiophene-3-carbaldehyde

CAS: 39856-98-9

2-Bromobenzo[b]thiophene-3-carbaldehyde is a copper (II) complex, which is obtained by the reaction of 2-bromobenzo[b]-thiophene with copper metal in an alkaline environment. It is a divalent organometallic compound with a formyl group. The complex has been synthesized and studied using spectroscopic methods. It has also been shown to be nucleophilic and can react with electrophiles, such as hydrosulfide, to produce thiols. The carbonyl group can undergo tautomerization to the enol form.

Formula: C₉H₅BrOS

Purity: Min. 95%

Molecular weight: 241.1 g/mol

Ref: 3D-PBA85698