5-Chloroindole, 98%

Code: C47604-1G D2-231

Not available outside of the UK & Ireland.

Application

5-Chloroindole has been used in the synthesis of 5-chloro-3-indole-N,N- dimethylglyoxalamide and 5-chloro-N,N-dimethyltryptamine. It may be used...


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Your Price
$67.91 1G
Discontinued

Not available outside of the UK & Ireland.

Application

5-Chloroindole has been used in the synthesis of 5-chloro-3-indole-N,N- dimethylglyoxalamide and 5-chloro-N,N-dimethyltryptamine. It may be used in the synthesis of dyestuffs in the presence of biocatalysts (Escherichia coli expressing multicomponent phenol hydroxylase (mPH) isolated from Pseudomonas sp. strains KL33 and KL28).

5-Chloroindole has been used to study the biotransformation of substituted indoles to indican derivatives in the tissue cultures of Polygonum tinctorium. It may be employed as a monomer in the preparation of redox-active film made up of a cyclic trimer and chains of linked cyclic trimer (polymer).

General description

5-Chloroindole can be synthesized by using 3-chlorobenzaldehyde as starting reagent.

5-Chloroindole is a 5-substituted indole. It undergoes electropolymerization to form a redox-active film consisting of a cyclic trimer and chains of linked cyclic trimer (polymer). It is a potential positive allosteric modulator (PAM) of the 5-HT3 receptor. It has been reported as strong inhibitor of the copper dissolution in acidic sodium chloride solution. It has been tested as corrosion inhibitor of mild steel in 1N deaerated sulphuric acid. Synthesis of 5-chloroindole, via nitration of indoline has been described.

Packaging

1, 5 g in glass bottle

assay98%
formcrystals
InChI keyMYTGFBZJLDLWQG-UHFFFAOYSA-N
InChI1S/C8H6ClN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H
mp69-71 °C (lit.)
Quality Level100
SMILES stringClc1ccc2[nH]ccc2c1
Cas Number17422-32-1
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