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246220

Sigma-Aldrich

4-Chloroindole

98%

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About This Item

Formula empirica (notazione di Hill):
C8H6ClN
Numero CAS:
25235-85-2
Peso molecolare:
151.59
Beilstein:
114880
Numero CE:
246-747-8
Numero MDL:
MFCD00005665
Codice UNSPSC:
12352100
ID PubChem:
24854796
NACRES:
NA.22

Saggio

98%

Indice di rifrazione

n20/D 1.628 (lit.)

P. eboll.

129-130 °C/4 mmHg (lit.)

Solubilità

ethanol: 50 mg/mL, clear, colorless

Densità

1.259 g/mL at 25 °C (lit.)

Stringa SMILE

Clc1cccc2[nH]ccc12

InChI

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

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Descrizione generale

The nitrosation rate of 4-chloroindole and the stability of its nitrosated products were studied.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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H G Tiedink et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 27(11), 723-730 (1989-11-01)
The nitrosation rates of indole-3-acetonitrile, indole-3-carbinol, indole and 4-chloroindole and the stability of their nitrosated products were investigated. Each of the nitrosated indole compounds was directly mutagenic to Salmonella typhimurium TA100 in the following order of potency: 4-chloroindole much greater
Zhong-Liu Wu et al.
The Journal of biological chemistry, 280(49), 41090-41100 (2005-10-11)
The natural product indole is a substrate for cytochrome P450 2A6. Mutagenesis of P450 2A6 was done to expand its capability in the oxidization of bulky substituted indole compounds, which are not substrates for the wild-type enzyme or the double
H G Tiedink et al.
Cell biology and toxicology, 7(4), 371-386 (1991-10-01)
4-chloro-methoxyindole is a naturally occurring compound in Vicia faba which can easily react with nitrite to form a N-nitroso compound. In this in vitro study, the potential genotoxic effects of nitrosated 4-chloro-6-methoxyindole and its structural analogue 4-chloroindole were evaluated for
Zhi-Gang Zhang et al.
Journal of biotechnology, 139(1), 12-18 (2008-11-06)
Cytochrome P450 (P450) 2A6 is able to catalyze indole hydroxylation to form the blue dye indigo. The wild-type P450 2A6 enzyme was randomly mutated throughout the whole open reading frame and screened using 4-chloroindole hydroxylation, a substituted indole selected from
Chaitany Jayprakash Raorane et al.
Biomolecules, 10(8) (2020-08-23)
Multi-drug resistant Acinetobacter baumannii is well-known for its rapid acclimatization in hospital environments. The ability of the bacterium to endure desiccation and starvation on dry surfaces for up to a month results in outbreaks of health care-associated infections. Previously, indole

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