84172
Salicylaldoxime
≥98.0% (NT)
Synonym(s):
2-Hydroxybenzaldehyde oxime
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About This Item
Linear Formula:
2-(HO)C6H4CH=NOH
CAS Number:
Molecular Weight:
137.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-353-8
Beilstein/REAXYS Number:
1859881
MDL number:
Assay:
≥98.0% (NT)
Form:
crystals
Quality Level
assay
≥98.0% (NT)
form
crystals
mp
57-59 °C, 59-61 °C (lit.)
functional group
amine, oxime
SMILES string
O\N=C\c1ccccc1O
InChI
1S/C7H7NO2/c9-7-4-2-1-3-6(7)5-8-10/h1-5,9-10H/b8-5+
InChI key
ORIHZIZPTZTNCU-VMPITWQZSA-N
Application
- Novel uncharged triazole salicylaldoxime derivatives as potential acetylcholinesterase reactivators: This research focuses on the synthesis and evaluation of novel salicylaldoxime derivatives, aimed at reactivating acetylcholinesterase inhibited by nerve agents (MH Baghersad, A Habibi, 2023).
- Selectivity of Salicylaldoxime and its Derivatives: This study utilizes Density Functional Theory (DFT) to examine the selectivity and effectiveness of salicylaldoxime derivatives in various chemical applications (B Tuzun, 2014).
- Synthesis and Spectroscopic study of Pd(II)-Salicylaldoxime complexes with amine ligands: This paper presents the synthesis and characterization of new Pd(II) complexes with salicylaldoxime, exploring their potential uses in catalysis and material science (EN Al_Sabawi et al., 2021).
Other Notes
Reagent for the spectrophotometric determination of Cu(II), Fe (III), Mo(VI) and Ni(II); a review
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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D D Ourth et al.
Developmental and comparative immunology, 6(1), 75-85 (1982-01-01)
Fresh channel catfish (Ictalurus punctatus) serum from unimmunized catfish exhibited 100% bactericidal activity against Salmonella paratyphi. Components responsible for bactericidal activity could be absorbed from the fresh catfish serum with S. paratyphi. The bactericidal system of the fresh catfish serum
F Minutolo et al.
Journal of medicinal chemistry, 44(24), 4288-4291 (2001-11-16)
The phenolic "A-ring" of natural and synthetic estrogen receptor (ER) ligands was effectively replaced by a planar six-member ring formed through an intramolecular hydrogen bond within a salicylaldoxime. Thus, oxime 1, a structural analogue of a triarylethylene estrogen, showed a
Ross S Forgan et al.
Chemical communications (Cambridge, England), (34)(34), 4049-4051 (2008-09-02)
Attaching dialkylaminomethyl arms to commercial phenolic oxime copper extractants yields reagents which transport base metal salts very efficiently by forming neutral 1:1 or 1:2 complexes with zwitterionic forms of the ligands.