| Weight | 279.915 g/mol |
|---|---|
| Formula | C7H4Br2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3,5-DIBROMOSALICYLALDEHYDE (90-59-5)
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- Synthesis, structures and urease inhibition studies of Schiff base metal complexes derived from 3,5-dibromosalicylaldehyde (European Journal of Medicinal Chemistry, 2012)
- A New Selective Preparation of 4H-Chromenes by Reaction of Alkyl Cyanoacetate with 3,5-Dibromosalicylaldehyde in the Presence of Ammonium Acetate (Synthesis, 1977)
- Studies on Halosalicylaldehyde. IV: Spectrophotometric Determination of Amino Acids by 3, 5-Dibromosalicylaldehyde@@@3,5- (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1961)
- Determination Of Cobalt (II) In Various Environmental Samples With 3,5-Dibromosalicylaldehyde Thiosemicarbazone Using Spectrophotometry Coupled With Flow-Injection Technique (Analytical chemistry, an Indian journal, 2006)
- Inhibition Performance of a New 3,5-dibromosalicylaldehyde-2-thenoyl Hydrazine Schiff Base for Carbon Steel in Oilfield Water and Relevant Molecular Dynamics Simulation (Journal of the Chinese Society of Corrosion and Protection, 2014)
- Studies on Halosalicylaldehyde. II: Spectrophotometric Determination of Primary Amines by 3, 5-Dibromosalicylaldehyde@@@3,5-Dibromosalicylaldehyde (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1959)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C=C(C(=C1Br)O)C=O)Br
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InChIKeyJHZOXYGFQMROFJ-UHFFFAOYSA-N
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Similar Compounds
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3,5-DIBROMOSALICYLALDEHYDE
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