Weight | 152.153 g/mol |
---|---|
Formula | C7H8N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3-Hydroxybenzohydrazide (5818-06-4)
5818-06-4
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- Synthesis and antitumor activity of (4-hydroxyphenyl)[5-substituted alkyl/aryl)-2-thioxo-1,3,4-thiadiazol-3-yl]methanone and [(3,4-disubstituted)-1,3-thiazol-2ylidene]-4-hydroxybenzohydrazide (Medicinal Chemistry Research, 2011)
- Synthesis, characterization, structural analysis of metal(II) complexes of N-[(E)-3-Bromo-5-Chloro-2-hydroxybenzidene]-4-hydroxybenzohydrazideMultisubstituted Schiff base as a F and Cu 2+ ions selective chemosensor (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2014)
- Synthesis, Antimycobacterial Activity and 3D QSAR Studies of Some New Derivatives of pHydroxybenzohydrazide (Qsar & Combinatorial Science, 2009)
- Synthesis, X-Ray Structural Characterization, and Catalytic Property of Dioxomolybdenum(VI) Complexes With N-(3-Bromo-2-hydroxybenzylidene)-2-hydroxybenzohydrazide and N-(5-Chloro-2-hydroxybenzylidene)-4- nitrobenzohydrazide (Synthesis and Reactivity in Inorganic Metal-organic and Nano-metal Chemistry, 2014)
- Synthesis, Structures, and Antimicrobial Activity of Two Schiff Bases Derived from 3-Hydroxybenzohydrazide and 3-Alkoxysalicylaldehyde (Polish Journal of Chemistry, 2008)
- 2-(3,5-Dichloro-2-hydroxybenzylidene)-2-hydroxybenzohydrazide (Acta Crystallographica Section E: Crystallographic Communications, 2007)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5818-06-4
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SMILESC1=CC(=CC(=C1)O)C(=O)NN
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InChIKeyOACGSLLKFCMXSX-UHFFFAOYSA-N
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Estimated Properties
Boiling Point | 285.21 C | EPA T.E.S.T. |
---|---|---|
Boiling Point | 359.94 C | EPI Suite |
Density | 1.3 g/cm3 | EPA T.E.S.T. |
Flash Point | 152.64 C | EPA T.E.S.T. |
Melting Point | 143.33 C | EPI Suite |
Water Solubility | 42534.9 mg/L | EPA T.E.S.T. |
Water Solubility | 1e+06 mg/L | EPI Suite |
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