Weight | 152.153 g/mol |
---|---|
Formula | C7H8N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
2-Hydroxybenzohydrazide (936-02-7)
salicyl hydrazide
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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, antibacterial and antifungal studies of some transition and rare earth metal complexes of N-benzylidene-2-hydroxybenzohydrazide (Bulletin of The Chemical Society of Ethiopia, 2011)
- A binuclear Zn(II)Zn(II) complex from a 2-hydroxybenzohydrazide-derived Schiff base for selective detection of pyrophosphate (Dalton Transactions, 2014)
- Structural, magnetic and optical properties of an FeIII dimer bridged by the meridional planar divergent N,N-bis(salicyl)hydrazide and its photo- and electro-chemistry in solution (Dalton Transactions, 2013)
- 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)
- N-[4-(dipropylamino)benzylidene]-2-hydroxybenzohydrazide is a dynamin GTPase inhibitor that suppresses cancer cell migration and invasion by inhibiting actin polymerization (Biochemical and Biophysical Research Communications, 2014)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - salicyl hydrazide
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SMILESC1=CC=C(C(=C1)C(=O)NN)O
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InChIKeyXSXYESVZDBAKKT-UHFFFAOYSA-N
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