CAS 5192-03-0
:5-Aminoindole
Description:
5-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 5th carbon of the indole ring. This compound is typically a white to light yellow solid and is known for its role in various chemical reactions and applications, particularly in the synthesis of pharmaceuticals and agrochemicals. It exhibits basic properties due to the presence of the amino group, allowing it to participate in hydrogen bonding and act as a nucleophile in chemical reactions. 5-Aminoindole can also undergo electrophilic substitution reactions, making it a versatile intermediate in organic synthesis. Additionally, it has been studied for its potential biological activities, including antimicrobial and anticancer properties. Its solubility varies depending on the solvent, and it is generally stable under standard laboratory conditions. Proper handling and storage are essential, as with many organic compounds, to ensure safety and maintain its integrity for research and application purposes.
Formula:C8H8N2
InChI:InChI=1S/C8H8N2/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H,9H2
InChI key:InChIKey=ZCBIFHNDZBSCEP-UHFFFAOYSA-N
SMILES:NC=1C=C2C(=CC1)NC=C2
Synonyms:- (Indol-5-yl)amine
- 1H-Indol-5-Amine
- 1H-Indol-5-ylamine
- 5-Amino Indole
- 5-Amino-1H-indole
- 5-Indolamine
- Indol-5-Ylamine
- Indole, 5-amino-
- NSC 61452
- 5-Aminoindole
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Found 8 products.
5-Aminoindole
CAS:Formula:C8H8N2Purity:>98.0%(GC)(T)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:132.171H-Indol-5-amine
CAS:<p>1H-Indol-5-amine (5-Aminoindole) is an indole derivative that can be used as an absorbent in (HCIC) and for the synthesis of tetracyclic heterocycles.</p>Formula:C8H8N2Purity:98.76%Color and Shape:SolidMolecular weight:132.165-Amino-1H-indole
CAS:<p>5-Amino-1H-indole</p>Formula:C8H8N2Purity:97%Color and Shape: very dark grey to black solidMolecular weight:132.16g/mol5-Aminoindole
CAS:<p>5-Aminoindole is a versatile chemical intermediate that can be used in the synthesis of many different types of compounds. It has been used as a building block for the synthesis of complex molecules, such as antibiotics and other pharmaceuticals. 5-Aminoindole is also useful in research because it is a reagent that can be used to study the reaction between proteins and nucleic acids. This chemical reacts with calf thymus DNA to produce 5-aminoindole phosphate, which can then react with an activated phosphate group on a protein or nucleic acid. 5-Aminoindole is a high quality reagent that will provide you with excellent results in your experiments.</p>Formula:C8H8N2Molecular weight:132.17 g/mol5-Aminoindole
CAS:<p>5-Aminoindole is a hydrogen bond acid. It has been shown to have an optimum concentration of 0.1 mM in the presence of 0.2 mM potassium chloride and 2 mM magnesium chloride, which is similar to the pH range for biological systems. 5-Aminoindole also acts as a competitive inhibitor of quinoline derivatives, such as chloroquine and hydroxychloroquine, which are used in the treatment of malaria and rheumatoid arthritis. The compound has been shown to be active against primary cells grown in culture, including mouse erythrocytes and human hepatocytes. When used with agarose gel electrophoresis or electrochemical impedance spectroscopy, 5-aminoindole shows excellent selectivity for kinases over other enzymes. 5-Aminoindole is not reactive under physiological conditions because it does not have any redox potentials that can be measured by Langmuir adsorption isother</p>Formula:C8H8N2Purity:Min. 97%Color and Shape:Brown PowderMolecular weight:132.16 g/mol
