| Weight | 215.046 g/mol |
|---|---|
| Formula | C8H7BrO2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-Bromophenylacetic acid (1878-68-8)
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- Conjugation of aspartic acid with 4-bromophenylacetic acid, an auxin analogue of aspartic acid (Phytochemistry, 1987)
- Influence of the diversified structural variations at the imine functionality of 4-bromophenylacetic acid derived hydrazones on alkaline phosphatase inhibition: synthesis and molecular modelling studies (RSC Advances, 2015)
- Microbial hydroxylation of o-bromophenylacetic acid: synthesis of 4-substituted-2,3-dihydrobenzofurans (Journal of Industrial Microbiology & Biotechnology, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1CC(=O)O)Br
-
InChIKeyQOWSWEBLNVACCL-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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19806-17-8
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(101-97-3)
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(5391-88-8)
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(14062-19-2)
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(73918-56-6)
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4-hydroxyphenylacetic acid
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4-Bromophenylacetonitrile
(16532-79-9)
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2-Naphthylacetic acid
(581-96-4)
1 alternate name
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(492-37-5)
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Methyl (4-cyanophenyl)acetate
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(99-90-1)
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(29519-77-5)
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(501-89-3)
1 alternate name
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(57676-50-3)
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3549-23-3
(3549-23-3)
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(4870-65-9)
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(23703-22-2)
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(45791-36-4)
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(223555-90-6)
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(331-25-9)
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51554-93-9
(51554-93-9)
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1-(4-bromophenyl)propan-1-ol
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4-Bromophenylacetic acid
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