5-Methylindole structure
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Common Name | 5-Methylindole | ||
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CAS Number | 614-96-0 | Molecular Weight | 131.17 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 269.0±9.0 °C at 760 mmHg | |
Molecular Formula | C9H9N | Melting Point | 60-62 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 114.7±11.3 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of 5-Methylindole5-Methylindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 5-Methylindole |
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Synonym | More Synonyms |
Description | 5-Methylindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 269.0±9.0 °C at 760 mmHg |
Melting Point | 60-62 °C(lit.) |
Molecular Formula | C9H9N |
Molecular Weight | 131.17 |
Flash Point | 114.7±11.3 °C |
Exact Mass | 131.073502 |
PSA | 15.79000 |
LogP | 2.60 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.655 |
Storage condition | Keep Cold |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
Precursor 10 | |
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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% |
NMR studies of the mode of binding of corepressors and inducers to Escherichia coli trp repressor.
Eur. J. Biochem. 235(3) , 804-13, (1996) The binding of the corepressors tryptophan and 5-methyltryptophan and of the inducers 3-indolepropionate, 3-indoleacrylate and 5-methylindole to the Escherichia coli trp repressor have been studied by... |
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Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis.
J. Med. Chem. 47(12) , 3236-41, (2004) Indigoids, a class of bis-indoles, represent a promising protein kinase inhibitor scaffold. Oxidation of indole by cytochrome P450 (P450) has been shown to generate species (indoxyl, isatin) that coup... |
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Mass analyzed threshold ionization spectroscopy of 5-methylindole and 3-methylindole cations and the methyl substitution effect.
J. Chem. Phys. 120(11) , 5057-63, (2004) The vibrationally resolved mass analyzed threshold ionization spectra of jetcooled 5-methylindole (5MI) and 3-methylindole (3MI) have been recorded by ionizing via various vibronic levels of each spec... |
6-methylindole |
5-methyl-indole |
5-Methylindole |
5-methyl indane-1,3-dione |
5-Methylindan-1,3-dion |
5-Methyl-1H-indole |
5-metyl-1H-indole |
Indole, 5-methyl- |
MFCD00005680 |
1H-Indole, 5-methyl- |
5-Methylindol |
EINECS 210-400-9 |
5-methyl indan-1,3-dione |