CAS 5192-23-4

4-Aminoindole

Description:

4-Aminoindole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring, with an amino group (-NH2) positioned at the 4th carbon of the indole ring. This compound is typically a white to light yellow solid and is known for its aromatic properties, contributing to its stability and reactivity. It is soluble in polar solvents such as water and alcohols, while being less soluble in non-polar solvents. 4-Aminoindole is of interest in various fields, including medicinal chemistry, due to its potential biological activities, such as anti-cancer and anti-inflammatory properties. The presence of the amino group allows for further chemical modifications, making it a versatile building block in organic synthesis. Additionally, it can participate in various chemical reactions, including electrophilic substitutions and coupling reactions, which are valuable in the development of pharmaceuticals and agrochemicals. Safety data indicates that, like many amines, it should be handled with care, as it may cause irritation upon contact with skin or eyes.

Formula: C₈H₈N₂

InChI: InChI=1/C8H8N2/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,9H2

SMILES: c1cc(c2cc[nH]c2c1)N

Synonyms:

• 1H-Indol-4-amin
• 1H-Indol-4-amine
• 1H-Indol-4-ylamine
• 4-Amino-1H-Indole
• Indole-4-Amine

4-Aminoindole

CAS: 5192-23-4

Formula: C₈H₈N₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 132.1625

Ref: IN-DA003KRE

4-Aminoindole

CAS: 5192-23-4

Formula: C₈H₈N₂

Molecular weight: 132.17

Ref: 7W-GK5199

4-Aminoindole

CAS: 5192-23-4

Formula: C₈H₈N₂

Purity: >98.0%(GC)

Color and Shape: White to Gray to Brown powder to crystal

Molecular weight: 132.17

Ref: 3B-A2070

4-Amino-1H-indole

CAS: 5192-23-4

4-Amino-1H-indole

Formula: C₈H₈N₂

Purity: 97%

Color and Shape: brown solid

Molecular weight: 132.16g/mol

Ref: 54-OR7782

4-Aminoindole

CAS: 5192-23-4

4-Aminoindole is a heterocycle with a carboxy group and four nitrogen atoms. It can be synthesized by reacting hydrochloric acid with nitrobenzene. 4-Aminoindole has shown potential as a drug target, which may be due to its ability to inhibit the enzyme carboxamidase. The compound is also acidic in water, making it an ideal candidate for use as an acid catalyst. Electropolymerization of 4-aminoindole has been achieved using Pt electrodes in the presence of an acidic environment. This reaction results in the formation of functional groups on the metal surface that are not found in most other electropolymerization reactions.

Formula: C₈H₈N₂

Color and Shape: Powder

Molecular weight: 132.16 g/mol

Ref: 3D-FA10290

1H-Indol-4-amine

CAS: 5192-23-4

Formula: C₈H₈N₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 132.166

Ref: 10-F023427

4-Aminoindole

CAS: 5192-23-4

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Formula: C₈H₈N₂

Molecular weight: 132.17 g/mol

Ref: 3D-A-5600