| Weight | 295.914 g/mol |
|---|---|
| Formula | C7H4Br2O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3,5-DIBROMOSALICYLIC ACID (3147-55-5)
3,5-dbsa
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- Alternative aspirins as antisickling agents: acetyl-3,5-dibromosalicylic acid. (Proceedings of the National Academy of Sciences of the United States of America, 1977)
- DBSA catalyzed cyclotrimerization of acetophenones: An efficient synthesis of 1,3,5-triarylbenzenes under solvent-free conditions (Comptes Rendus Chimie, 2013)
- DFT computations, vibrational spectra, monomer, dimer, NBO and NMR analyses of antifungal agent: 3,5-Dibromosalicylic acid (Journal of Molecular Structure, 2012)
- Allosteric Inhibition of Endothelin ETA Receptors by 3,5-Dibromosalicylic Acid (Molecular Pharmacology, 2000)
- Ground- and excited-state intramolecular proton transfer in 3,5-dibromosalicylic acid (Journal of Molecular Structure, 2003)
- Attempted synthesis of esters of tricarballylic acid and 3,5-dibromosalicylic acid. Structure and properties of tricarballylic acid, its anhydrides and some of their derivatives, and an investigation of the reaction pathways of anhydride formation by 1H NMR spectroscopy, MNDO and molecular mechanics methods (Journal of The Chemical Society-perkin Transactions 1, 1991)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,5-dbsa
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SMILESC1=C(C=C(C(=C1Br)O)C(=O)O)Br
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InChIKeyBFBZHSOXKROMBG-UHFFFAOYSA-N
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Similar Compounds
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alpha,3,5-Tribromo-2-hydroxytoluene
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5-Methoxysalicylic acid
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4-bromo-2-(hydroxymethyl)-6-methoxyphenol
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3,5-DIBROMOSALICYLIC ACID
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