| Weight | 196.047 g/mol |
|---|---|
| Formula | C8H6BrN |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
5-BROMOINDOLE (10075-50-0)
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- Electrosyntheses and characterization of poly(5-bromoindole) in boron trifluoride diethyl etherate (Journal of Applied Polymer Science, 2006)
- In vivo characterization of horseradish peroxidase with indole-3-acetic acid and 5-bromoindole-3-acetic acid for gene therapy of cancer (Cancer Gene Therapy, 2010)
- Experimental thermochemical study of 5-bromoindole and 5-bromoindoline (The Journal of Chemical Thermodynamics, 2009)
- 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=CC2=C(C=CN2)C=C1Br
-
InChIKeyVXWVFZFZYXOBTA-UHFFFAOYSA-N
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