| Weight | 199.047 g/mol |
|---|---|
| Formula | C8H7BrO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4'-Bromoacetophenone (99-90-1)
p-bromoacetophenone · 4-bromoacetophenone
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- Palladium-catalyzed carbonylation of aryl halides a detailed investigation of the alkoxycarbonylation of 4-bromoacetophenone (Journal of Molecular Catalysis A-chemical, 2000)
- FT-IR and FT-Raman spectral investigation, computed IR intensity and Raman activity analysis and frequency estimation analysis on 4-chloro-2-bromoacetophenone using HF and DFT calculations. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- Bromoacetophenone-based photonucleases: photoinduced cleavage of DNA by 4'-bromoacetophenone-pyrrolecarboxamide conjugates. (Organic Letters, 1999)
- A versatile tandem retro-[1,4]-Brook rearrangement-condensation reaction of o-bromoacetophenone silyl enol ethers (Tetrahedron Letters, 1999)
- Green Route to the 2,6-Disubstituted Imidazo[2,1-b]-1,3,4-Thiadiazoles by the Cyclocondensation of -Bromoacetophenone Derivative and 1,3,4- Thiadiazoles Using Ionic Liquids (Letters in Organic Chemistry, 2006)
- The reaction of carbon disulfide with bromoacetophenone in the presence of primary amines: synthesis of 3-alkyl-4-phenyl-1,3-thiazole-2(3H)-thione derivatives (Journal of Sulfur Chemistry, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - p-bromoacetophenone
- 4-bromoacetophenone
-
SMILESCC(=O)C1=CC=C(C=C1)Br
-
InChIKeyWYECURVXVYPVAT-UHFFFAOYSA-N
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