| Identification | More | [Name]
Salicylhydrazide | [CAS]
936-02-7 | [Synonyms]
2-HYDROXYBENZENE-1-CARBOHYDRAZIDE
2-HYDROXYBENZHYDRAZIDE
2-HYDROXY-BENZOIC ACID HYDRAZIDE
2-HYDROXYBENZOIC HYDRAZIDE
2-HYDROXYBENZOYLHYDRAZINE
AKOS BC-3011
LABOTEST-BB LT00000145
O-HYDROXYBENZHYDRAZIDE
O-HYDROXYBENZOYLHYDRAZINE
SALICYL HYDRAZIDE
SALICYLIC ACID HYDRAZIDE
SALICYLIC HYDRAZIDE
SALICYLOYL HYDRAZIDE
TIMTEC-BB SBB007759
2-Hydroxybenzenecarboxylic acid hydrazide
2-Hydroxybenzohydrazide
2-hydroxy-benzoicacihydrazide
2-Hydroxybenzoylhydrazide
o-Hydroxybenzoic acid hydrazide
o-Hydroxybenzoic hydrazide | [EINECS(EC#)]
213-311-3 | [Molecular Formula]
C7H8N2O2 | [MDL Number]
MFCD00007599 | [Molecular Weight]
152.15 | [MOL File]
936-02-7.mol |
| Hazard Information | Back Directory | [Chemical Properties]
WHITE TO OFF-WHITE CRYSTALLINE POWDER | [Uses]
A novel colorimetric probe, CDAH, was designed and synthesized using a coumarin derivative as the fluorescent moiety and salicylhydrazide as the ligand through a Schiffs reaction.[2] | [Application]
2-hydroxybenzohydrazide is a useful research chemical. | [Preparation]
The preparation of salicylhydrazide was carried out according to the literature. To a solution of methyl salicylate (0.1 mol, 13.81 g) in 30 mL of absolute alcohol in a 150 mL three-neck flask, hydrazine hydrate (30 mL, 80%) was added. The reaction mixture was then heated to reflux for 4 hours. Next, the excess absolute alcohol was completely removed under reduced pressure. The residue was recrystallized from water to yield salicylhydrazide.[1] | [References]
[1] Meng, D., Liu, F., Li, Y., Yang, Z., Li, G., & Guo, D. (2015). Synthesis, characterization and properties of salicylhydrazide–salicylacylhydrazone derivatives and their terbium complexes. Luminescence, 31 2, 507–514. https://doi.org/10.1002/bio.2989 |
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