| Weight | 196.047 g/mol |
|---|---|
| Formula | C8H6BrN |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-Bromoindole (52415-29-9)
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- Synthesis of 6- and 7-arylindoles via palladium-catalyzed cross-coupling of 6- and 7-bromoindole with arylboronic acids (Synlett, 1994)
- 6-Bromoindole-3-Carbaldehyde, from an Acinetobacter Sp. Bacterium Associated with the Ascidian Stomozoa murrayi (Journal of Chemical Ecology, 1997)
- Ethyl 6-Bromo-3indolcarboxylate and 3-Hydroxyacetal-6-bromoindole, novel bromoindoles from the sponge Pleroma menoui of the Coral Sea (Zeitschrift fr Naturforschung, 1989)
- Synthesis and studies on antimicrobial, antiinflammatory and antiproliferative activities of heterocycles derived from 4-/5-/6-/7-nitro/5-fluoro/chloro/bromoindole-2-carbohydrazides (Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry, 2009)
- Synthesis and biological activity of 5-oxy-6-bromoindole substitutes (Pharmaceutical Chemistry Journal, 1988)
- Inhibitors of the early stages of virus-cell interactions among derivatives of 3-ethoxycarbonyl-5-hydroxy-6-bromoindole (Pharmaceutical Chemistry Journal, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC2=C1C=CN2)Br
-
InChIKeyMAWGHOPSCKCTPA-UHFFFAOYSA-N
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