| Weight | 185.064 g/mol |
|---|---|
| Formula | C8H9Br |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
1-Bromo-3-ethylbenzene (2725-82-8)
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- Poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) and N,N,N,N-tetrabromobenzene-1,3-disulfonamide as efficient reagents for synthesis of quinolines (Tetrahedron Letters, 2009)
- N,N,N^{\prime },N^{\prime }-Tetrabromobenzene-1,3-disulfonamide and poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) as new and efficient catalysts for the synthesis of highly substituted 1,6-dihydropyrazine-2,3-dicarbonitrile derivatives (Molecular Diversity, 2013)
- N,N,N,N-Tetrabromobenzene-1,3-disulfonamide and Poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) as Mild and Efficient Catalysts for Solvent-free Synthesis ofN-Cyclohexyl-2-aryl(alkyl)-imidazo[1,2-a]pyridin-3-amine Derivatives: Mild Synthesis ofN-Cyclohexyl-2-aryl(alkyl)-imidazo[1,2-a]pyridin-3-amine (Journal of Heterocyclic Chemistry, 2014)
- ChemInform Abstract: Poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) and N,N,N,N-Tetrabromobenzene-1,3-disulfonamide as Efficient Reagents for the Synthesis of Quinolines. (ChemInform, 2009)
- ChemInform Abstract: N,N,N,N-Tetrabromobenzene-1,3-disulfonamide and Poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) as Mild and Efficient Catalysts for Solvent-Free Synthesis of N-Cyclohexyl-2-aryl(alkyl)-imidazo[1,2-a]pyridin-3-amine Derivatives (IV) (ChemInform, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC1=CC(=CC=C1)Br
-
InChIKeyZRFJYAZQMFCUIX-UHFFFAOYSA-N
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