![]() 4-Aminoindole structure
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Common Name | 4-Aminoindole | ||
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CAS Number | 5192-23-4 | Molecular Weight | 132.163 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 354.0±15.0 °C at 760 mmHg | |
Molecular Formula | C8H8N2 | Melting Point | 106-109 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 195.0±7.6 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Synthesis and in vitro and in vivo antitumor activity of 2-phenylpyrroloquinolin-4-ones.
J. Med. Chem. 48(9) , 3417-27, (2005) In our search for potential new anticancer drugs, we designed and synthesized a series of tricyclic compounds containing the antimitotic 2-phenylazaflavone chromophore fused to a pyrrole ring in a pyrroloquinoline structure. Compounds 8, 18, 19, 22, 23, 25 an... |
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Cytokinin activity of azaindene, azanaphthalene, naphthalene, and indole derivatives. Torigoe Y, et al.
Phytochemistry 11(5) , 1623-1630, (1972)
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Synthestic approaches to the teleocidin-related tumour promoters: a total synthesis of (±)-indolactam V. de Laszlo SE, et al.
J. Chem. Soc. Chem. Commun. 4 , 344-346., (1986)
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An efficient synthesis of azidoindoles and azidotryptophans. Melhado LL and Leonard NJ.
J. Org. Chem. 48(25) , 5130-5133, (1983)
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