CAS 827-01-0
:5-Chloroindole-3-carboxaldehyde
Description:
5-Chloroindole-3-carboxaldehyde is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a chloro group at the 5-position and an aldehyde functional group at the 3-position significantly influences its chemical reactivity and properties. This compound typically appears as a solid or crystalline substance and is known for its potential applications in medicinal chemistry, particularly in the synthesis of various bioactive molecules. It may exhibit biological activities due to the indole moiety, which is a common scaffold in many pharmaceuticals. The compound is soluble in organic solvents, and its reactivity can be attributed to the electrophilic nature of the aldehyde group, allowing it to participate in various chemical reactions, such as condensation and nucleophilic addition. Safety precautions should be taken when handling this compound, as it may pose health risks, including irritation or toxicity. Proper storage and disposal methods are essential to ensure safety in laboratory settings.
Formula:C9H6ClNO
InChI:InChI=1/C9H6ClNO/c10-7-1-2-9-8(3-7)6(5-12)4-11-9/h1-5,11H
SMILES:c1cc2c(cc1Cl)c(c[nH]2)C=O
Synonyms:- 1H-indole-3-carboxaldehyde, 5-chloro-
- 5-Chloro-1H-indole-3-carbaldehyde
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Found 5 products.
5-Chloroindole-3-carboxaldehyde
CAS:Formula:C9H6ClNOPurity:96%Color and Shape:SolidMolecular weight:179.60305-Chloroindole-3-carboxaldehyde
CAS:Formula:C9H6ClNOPurity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:179.605-Chloroindole-3-carboxaldehyde
CAS:<p>5-Chloroindole-3-carboxaldehyde</p>Formula:C9H6ClNOPurity:≥95%Color and Shape: light orange powderMolecular weight:179.60g/mol5-Chloroindole-3-carboxaldehyde
CAS:Formula:C9H6ClNOPurity:96%Color and Shape:SolidMolecular weight:179.65-Chloroindole-3-carboxaldehyde
CAS:<p>5-Chloroindole-3-carboxaldehyde is a synthetic antiplatelet drug. It is an acceptor that forms base with streptochlorin, which is the donor. The molecular modelling of this chemical has shown that it binds to the amide group of amicetin, which is a molecule in the phyla Actinobacteria. This binding inhibits the activity of amicetin and leads to a low detection of streptochlorin by high performance liquid chromatography (HPLC). 5-Chloroindole-3-carboxaldehyde has been shown to inhibit platelet aggregation in vitro, as well as inhibit the growth of Streptococcus pyogenes and other bacteria.</p>Formula:C9H6ClNOPurity:Min. 95%Molecular weight:179.6 g/mol




