![]() 4-Chloroindole structure
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Common Name | 4-Chloroindole | ||
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CAS Number | 25235-85-2 | Molecular Weight | 151.593 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 293.0±13.0 °C at 760 mmHg | |
Molecular Formula | C8H6ClN | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 158.9±5.4 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Use of 4-Chloroindole |
Name | 4-Chloroindole |
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Synonym | More Synonyms |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 293.0±13.0 °C at 760 mmHg |
Molecular Formula | C8H6ClN |
Molecular Weight | 151.593 |
Flash Point | 158.9±5.4 °C |
Exact Mass | 151.018875 |
PSA | 15.79000 |
LogP | 2.74 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.688 |
Storage condition | 2-8°C |
Stability | Store in Refrigerator |
Water Solubility | insoluble |
Symbol |
![]() GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xn:Harmful |
Risk Phrases | R20/21/22;R36/37/38 |
Safety Phrases | S26-S36-S36/37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
Precursor 7 | |
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DownStream 10 | |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
The stability of the nitrosated products of indole, indole-3-acetonitrile, indole-3-carbinol and 4-chloroindole.
Food Chem. Toxicol. 27(11) , 723-30, (1989) 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 w... |
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In-vitro testing and the carcinogenic potential of several nitrosated indole compounds.
Cell Biol. Toxicol. 7(4) , 371-86, (1991) 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 nitr... |
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Expansion of substrate specificity of cytochrome P450 2A6 by random and site-directed mutagenesis.
J. Biol. Chem. 280(49) , 41090-100, (2005) 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 sub... |
4-Chloroindole |
1H-Indole, 4-chloro- |
1H-Indole,4-chloro |
EINECS 246-747-8 |
4-Chloro-1H-indole |
Indole,4-chloro |
MFCD00005665 |
4-chloro-indole |