7-Bromo-1H-indole
7-Bromo-1H-indole structure
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Common Name | 7-Bromo-1H-indole | ||
|---|---|---|---|---|
| CAS Number | 51417-51-7 | Molecular Weight | 196.044 | |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 316.9±15.0 °C at 760 mmHg | |
| Molecular Formula | C8H6BrN | Melting Point | 41-44 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 145.5±20.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Multicomponent phenol hydroxylase-catalysed formation of hydroxyindoles and dyestuffs from indole and its derivatives.
Lett. Appl. Microbiol. 41(2) , 163-8, (2005) To establish multicomponent phenol hydroxylases (mPHs) as novel biocatalysts for producing dyestuffs and hydroxyindoles such as 7-hydroxyindole (7-HI) from indole and its derivatives.We have isolated Pseudomonas sp. KL33, which possesses a phenol degradation ... |
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Indole and 7-benzyloxyindole attenuate the virulence of Staphylococcus aureus.
Appl. Microbiol. Biotechnol. 97(10) , 4543-52, (2013) Human pathogens can readily develop drug resistance due to the long-term use of antibiotics that mostly inhibit bacterial growth. Unlike antibiotics, antivirulence compounds diminish bacterial virulence without affecting cell viability and thus, may not lead ... |
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Diversity Oriented Synthesis: Concise Entry to Novel Derivatives of Yohimbine and Corynanthe Alkaloids.
Tetrahedron Lett. 53(5) , 477-479, (2012) A novel MCAP-cycloaddition sequence has been applied to the facile synthesis of _-carboline intermediates to gain rapid access to novel derivatives of yohimbine-like and corynanthe-like compounds that may be easily diversified by cross-coupling reactions and ... |
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Total synthesis of indoles from Tricholoma species via Bartoli/heteroaryl radical methodologies.
J. Org. Chem. 66(2) , 638-41, (2001)
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The structure of monobrominated ethyl indole-3-carboxylate and the preparation of 7-bromoindole. Leggetter BE and Brown RK.
Can. J. Chem. 38(9) , 1467-1471, (1960)
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