CAS 5192-04-1
:7-Aminoindole
Description:
7-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 7th carbon of the indole framework. This compound typically appears as a solid and is known for its potential applications in pharmaceuticals and organic synthesis. It exhibits basic properties due to the presence of the amino group, which can participate in hydrogen bonding and act as a nucleophile in various chemical reactions. 7-Aminoindole is also recognized for its role in the synthesis of various bioactive molecules and can serve as a building block in the development of new drugs. Its reactivity can be influenced by the electronic properties of the indole ring, making it a versatile intermediate in organic chemistry. Additionally, it may exhibit fluorescence, which can be useful in biological imaging applications. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C8H8N2
InChI:InChI=1/C8H8N2/c9-7-3-1-2-6-4-5-10-8(6)7/h1-5,10H,9H2
SMILES:c1cc2cc[nH]c2c(c1)N
Synonyms:- 7-Indolamine
- 1H-indol-7-amine
- 1H-INDOL-7-YLAMINE
- 7-Amino-1H-indole 97%
- 7-Amino-1H-indole
- 7-AMINOINDOLE
- 7-Aminoindole 5192-4-1
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Found 6 products.
1H-Indol-7-amine
CAS:Formula:C8H8N2Purity:>98.0%(GC)Color and Shape:Orange to Brown to Dark purple powder to crystalMolecular weight:132.177-Amino-1H-indole
CAS:<p>7-Amino-1H-indole</p>Formula:C8H8N2Purity:97%Color and Shape: light brown to brown solidMolecular weight:132.16g/mol7-Aminoindole
CAS:Controlled Product<p>Applications 7-Aminoindole<br></p>Formula:C8H8N2Color and Shape:NeatMolecular weight:132.161H-Indol-7-amine
CAS:<p>1H-Indol-7-amine is a molecule that belongs to the group of basic proteins. It has been shown to be an optimum concentration for biological activity and can be used in the treatment of diseases such as cancer and diabetes. 1H-Indol-7-amine binds to acidic molecules and exhibits redox potentials that are suitable for hydrogen bond formation with other molecules. The molecule is also involved in protein kinase selectivity, which may be due to its ability to bind with nitrogen atoms. 1H-Indol-7-amine has been shown to have beneficial effects on agarose gels through x-ray crystal structures and has a number of favorable electrochemical properties, including low charge transfer resistance, high electron mobility, and good chemical stability.</p>Formula:C8H8N2Purity:Min. 95%Molecular weight:132.16 g/mol





