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C47604

Sigma-Aldrich

5-Chloroindole

98%

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About This Item

Formula empirica (notazione di Hill):
C8H6ClN
Numero CAS:
17422-32-1
Peso molecolare:
151.59
Beilstein:
2651
Numero CE:
241-448-9
Numero MDL:
MFCD00005672
Codice UNSPSC:
12352100
ID PubChem:
24892721
NACRES:
NA.22

Saggio

98%

Forma fisica

crystals

Punto di fusione

69-71 °C (lit.)

Stringa SMILE

Clc1ccc2[nH]ccc2c1

InChI

1S/C8H6ClN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H
MYTGFBZJLDLWQG-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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.

Applicazioni

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).

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Xiaoxue Tong et al.
Microbial cell factories, 15(1), 180-180 (2016-10-23)
Engineering of single-species biofilms for enzymatic generation of fine chemicals is attractive. We have recently demonstrated the utility of an engineered Escherichia coli biofilm as a platform for synthesis of 5-halotryptophan. E. coli PHL644, expressing a recombinant tryptophan synthase, was
Fluorescence properties of electropolymerised 5-substituted indoles in solution.
Jennings P, et al.
J. Chem. Soc., Faraday Trans., 94(24), 3619-3624 (1998)
Indole and 5-chloroindole as inhibitors of anodic dissolution and cathodic deposition of copper in acidic chloride solutions.
Scendo M, et al.
J. Appl. Electrochem., 33(3-4), 287-293 (2003)
5-Amino-and 5-chloro-indole as mild steel corrosion inhibitors in 1 N sulphuric acid.
Moretti G, et al.
Electrochimica Acta, 41(13), 1971-1980 (1996)
Indigo and indirubin derivatives from indoles in Polygonum tinctorium tissue cultures.
Shim JY, et al.
Biotechnology Letters, 20(12), 1139-1143 (1998)
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