| Weight | 196.047 g/mol |
|---|---|
| Formula | C8H6BrN |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-Bromoindole (52488-36-5)
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- An interesting regioselectivity of palladation for bromoindole derivatives : a convenient one-step synthesis of 4-bromodehydrotryptophan derivatives (Heterocycles, 1990)
- 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)
- ChemInform Abstract: Transformations of 1-Aryl-2-methyl-3-ethoxycarbonyl-4,5-dihydroxy-6- bromoindole Derivatives. (ChemInform, 1988)
- ChemInform Abstract: Synthesis and Biological Activity of 1-Alkyl(Aryl)-5-methoxy(4,5-dimethoxy)-6-bromoindole Derivatives. (ChemInform, 1987)
- ChemInform Abstract: Synthetic Studies of Indoles and Related Compounds. Part 23. An Interesting Regioselectivity of Palladation for Bromoindole Derivatives: A Convenient One-Step Synthesis of 4-Bromodehydrotryptophan Derivatives. (ChemInform, 1990)
- Synthesis of 4-Bromoindole Derivatives (Chinese Journal of Synthetic Chemistry, 2008)
-
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(=C1)Br
-
InChIKeyGRJZJFUBQYULKL-UHFFFAOYSA-N
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