Weight | 201.019 g/mol |
---|---|
Formula | C7H5BrO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
5-Bromosalicylaldehyde (1761-61-1)
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- Vanadium(V) complexes with salicylaldehyde semicarbazone derivatives bearing in vitro anti-tumor activity toward kidney tumor cells (TK-10): crystal structure of [VVO2(5-bromosalicylaldehyde semicarbazone)]. (Journal of Inorganic Biochemistry, 2005)
- Synthesis, spectral characterization, solution equilibria, in vitro antibacterial and cytotoxic activities of Cu(II), Ni(II), Mn(II), Co(II) and Zn(II) complexes with Schiff base derived from 5-bromosalicylaldehyde and 2-aminomethylthiophene. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- MIXED LIGAND COMPLEXES OF ALKALINE EARTH METALS: PART-X. Mg(II), Ca(II), Sr(II) and Ba(II) COMPLEXES WITH 5-BROMOSALICYLALDEHYDE AND b-DIKETONES (Journal of The Chilean Chemical Society, 2003)
- Unsymmetrical tetradentate Schiff base complexes derived from 2,3-diaminophenol and salicylaldehyde or 5-bromosalicylaldehyde (Transition Metal Chemistry, 2006)
- Direct and Derivative Spectrophotometric Determination of Copper(II) with 5-Bromosalicylaldehyde Thiosemicarbazone (The Open Analytical Chemistry Journal, 2009)
- Copper(II) and molybdenum(VI) complexes with 5-bromosalicylaldehyde S-allylisothiosemicarbazone: Syntheses, characterizations and crystal structures (Journal of Coordination Chemistry, 2013)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(C=C1Br)C=O)O
-
InChIKeyMKKSTJKBKNCMRV-UHFFFAOYSA-N
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