CAS 13414-56-7

2,3-DIHYDROBENZO[B]FURAN-7-YLAMINE

Description:

2,3-Dihydrobenzo[b]furan-7-ylamine, with the CAS number 13414-56-7, is an organic compound characterized by its fused ring structure, which includes a dihydrobenzo[b]furan moiety and an amine functional group. This compound typically exhibits properties associated with both aromatic and aliphatic systems due to its unique structure. It is likely to be a colorless to pale yellow solid or liquid, depending on its purity and specific conditions. The presence of the amine group suggests that it may engage in hydrogen bonding, influencing its solubility in polar solvents. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its reactivity can be attributed to the amine functionality, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₈H₉NO

2,3-Dihydrobenzofuran-7-amine

CAS: 13414-56-7

2,3-Dihydrobenzofuran-7-amine

Formula: C₈H₉NO

Purity: 95%

Molecular weight: 135.16

Ref: IN-DG240888

2,3-Dihydrobenzo[b]furan-7-ylamine

CAS: 13414-56-7

2,3-Dihydrobenzo[b]furan-7-ylamine

Formula: C₈H₉NO

Purity: 98%

Molecular weight: 135.16316

Ref: 54-OR958944

2,3-Dihydrobenzo[b]furan-7-ylamine

CAS: 13414-56-7

Formula: C₈H₉NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 135.1632

Ref: IN-DA0037UD

2,3-Dihydrobenzofuran-7-amine

CAS: 13414-56-7

Formula: C₈H₉NO

Purity: 95%

Color and Shape: Solid

Molecular weight: 135.166

Ref: 10-F339973

2,3-Dihydro-1-benzofuran-7-amine

CAS: 13414-56-7

2,3-Dihydro-1-benzofuran-7-amine is an industrial chemical that is used in the synthesis of a variety of pharmaceuticals. It serves as a protonic inhibitor and has been shown to be effective against acetaldehyde. This compound has been optimized for use in Friedel-Crafts reactions and can be used as a catalyst for hydroxylation reactions. 2,3-Dihydro-1-benzofuran-7-amine can be prepared by reductive amination of phenylacetic acid with formaldehyde followed by hydrolysis of the intermediate dihydropyridine.

Formula: C₈H₉NO

Purity: Min. 95%

Molecular weight: 135.17 g/mol

Ref: 3D-NAA41456