Weight | 191.013 g/mol |
---|---|
Formula | C7H4Cl2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3,5-Dichlorosalicylaldehyde (90-60-8)
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- EPR and electrochemical study of nickel(III) complexes of bis(3,5-dichlorosalicylaldehyde) o-phenylenediimine. Evidence for adduct formation with pyridines (Inorganic Chemistry, 1990)
- The asymmetric ONNO complexes of dioxouranium(VI) with N1,N4-diarylidene-S-propyl-thiosemicarbazones derived from 3,5-dichlorosalicylaldehyde: Synthesis, spectroscopic and structural studies (Polyhedron, 2011)
- Temperature dependence of proton magnetic resonance solvent shifts. 3,5-Dichlorosalicylaldehyde in carbon tetrachloride and benzene (Canadian Journal of Chemistry, 1968)
- Extraction-spectrophotometric determination of palladium(II) with 3,5-dichlorosalicylaldehyde-4-phenyl-3-thiosemicarbazone (Analyst, 1985)
- The structure of the hydrated salt of 3,5-dichlorosalicylaldehyde and 4-aminopyridine, C5H7N2+.C7H3Cl2O2.H2O (Acta Crystallographica Section C-crystal Structure Communications, 1983)
- c-Thioacylation by the WillgerodtKindler reaction. Structure of the anomalous products from salicylaldehydes. X-Ray crystal structure of the betaine from 1,2-dimethyl-1,4,5,6-tetrahydropyrimidine, sulphur, and 3,5-dichlorosalicylaldehyde (Journal of The Chemical Society-perkin Transactions 1, 1984)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C=C(C(=C1Cl)O)C=O)Cl
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InChIKeyFABVMBDCVAJXMB-UHFFFAOYSA-N
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