CAS 1196-69-6

5-Formylindole

Description:

5-Formylindole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a formyl group (-CHO) at the 5-position of the indole ring distinguishes it from other indole derivatives. This compound typically appears as a solid or crystalline substance and is known for its potential applications in organic synthesis and medicinal chemistry. It can participate in various chemical reactions, including condensation and substitution reactions, making it a valuable intermediate in the synthesis of more complex molecules. 5-Formylindole may exhibit biological activity, which has garnered interest in the field of drug discovery. Its properties, such as solubility and reactivity, can vary depending on the solvent and conditions used. As with many indole derivatives, it may also display fluorescence, which can be useful in analytical applications. Safety data should be consulted before handling, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₉H₇NO

InChI: InChI=1/C9H7NO/c11-6-7-1-2-8-3-4-10-9(8)5-7/h1-6,10H

InChI key: ADZUEEUKBYCSEY-UHFFFAOYSA-N

SMILES: c1cc2cc[nH]c2cc1C=O

Synonyms:

• Indole-5-carboxaldehyde
• 1H-indole-5-carbaldehyde
• 1H-indole-6-carbaldehyde
• 5-Indolealdehyde
• 1H-Indole-5-carboxaldehyde

Indole-5-carboxaldehyde

CAS: 1196-69-6

Formula: C₉H₇NO

Purity: >98.0%(GC)

Color and Shape: White to Yellow to Orange powder to crystal

Molecular weight: 145.16

Ref: 3B-I0674

Indole-5-carboxaldehyde, 98%

CAS: 1196-69-6

Indole-5-carboxaldehyde is used as a reactant in preparation of curcumin derivatives as anti-proliferative anti-inflammatory agents; and in synthesis of para-para stilbenophanes by McMurry coupling. It is also used as a reactant in stereoselective synthesis of dibenzylideneacetone derivatives as -a

Formula: C₉H₇NO

Purity: 98%

Color and Shape: Pale cream to cream to orange, Powder

Molecular weight: 145.16

Ref: 02-B25517

1H-Indole-5-carboxaldehyde

CAS: 1196-69-6

1H-Indole-5-carboxaldehyde

Formula: C₉H₇NO

Purity: 98%

Color and Shape: Solid

Molecular weight: 145.15798

Ref: 54-OR10488

Indole-5-carboxaldehyde (5-Formylindole)

CAS: 1196-69-6

Formula: C₉H₇NO

Molecular weight: 145.16

Ref: 7W-GK7389

1H-Indole-5-carboxaldehyde

CAS: 1196-69-6

Formula: C₉H₇NO

Purity: 98%

Color and Shape: Solid

Molecular weight: 145.1580

Ref: IN-DA000P9A

Indole-5-carboxaldehyde

Controlled Product

CAS: 1196-69-6

Formula: C₉H₇NO

Color and Shape: Neat

Molecular weight: 145.16

Ref: TR-I615010

Indole-5-carboxaldehyde

CAS: 1196-69-6

Indole-5-carboxaldehyde

Formula: C₉H₇NO

Purity: 98%

Molecular weight: 145.16

Ref: IN-DG7457

5-Formylindole

CAS: 1196-69-6

5-Formylindole is a non-selective and irreversible inhibitor of protein α, which is the catalytic subunit of the enzyme AMP-activated protein kinase. It binds to the hydroxyl group at position Cys177 in the ATP binding pocket of protein α, thereby inhibiting its activity. 5-Formylindole has been shown to inhibit tumor growth in xenografts and also inhibits fat accumulation in 3T3-L1 preadipocytes by inhibition of fatty acid synthesis. This compound has also been used to study molecular modeling in order to understand hydrogen bond interactions between aldehyde groups and intramolecular hydrogen. The genus that this compound belongs to is stilbene derivatives.

Formula: C₉H₇NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 145.16 g/mol

Ref: 3D-FF16209

5-Formylindole

CAS: 1196-69-6

Formula: C₉H₇NO

Purity: 98%

Color and Shape: Solid

Molecular weight: 145.161

Ref: 10-F016156