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
InChI key
ORIHZIZPTZTNCU-VMPITWQZSA-N
InChI
1S/C7H7NO2/c9-7-4-2-1-3-6(7)5-8-10/h1-5,9-10H/b8-5+
SMILES string
O\N=C\c1ccccc1O
assay
≥98.0% (NT)
form
crystals
mp
57-59 °C, 59-61 °C (lit.)
functional group
amine, oxime
Quality Level
Related Categories
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
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
84172-VAR: + 84172-500G: + 84172-INTR: + 84172-BULK: + 84172-100G:
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Hui-Lien Tsai et al.
Inorganic chemistry, 51(24), 13171-13180 (2012-12-12)
Two Mn(4) single-molecule-magnet (SMM)-based coordination polymers, {[Mn(4)O(salox)(3)(N(3))(3)(DMF)(2)(H(2)O)(dpp)]·0.5MeOH}(n) (1·0.5MeOH; H(2)salox = salicylaldoxime; dpp = 1,3-di-4-pyridylpropane; DMF = N,N-dimethylformamide) and {[Mn(4)O(Me-salox)(3)(N(3))(3)(dpp)(1.5)]·1.5Et(2)O}(n) (2·1.5Et(2)O; Me-H(2)salox = hydroxyphenylethanone oxime), are self-assembled from Mn(ClO(4))(2)·6H(2)O/H(2)salox and Mn(ClO(4))(2)·6H(2)O/Me-H(2)salox systems with dpp and NaN(3) in DMF/MeOH, respectively. Both compounds
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
Ian A Gass et al.
Dalton transactions (Cambridge, England : 2003), (15)(15), 2043-2053 (2008-04-03)
The synthesis and magnetic properties of the compounds [HNEt(3)][Fe(2)(OMe)(Ph-sao)(2) (Ph-saoH)(2)].5MeOH (1.5MeOH), [Fe(3)O(Et-sao)(O(2)CPh)(5)(MeOH)(2)].3MeOH (2.3MeOH), [Fe(4)(Me-sao)(4)(Me-saoH)(4)] (3), [HNEt(3)](2)[Fe(6)O(2)(Me-sao)(4)(SO(4))(2)(OMe)(4)(MeOH)(2)] (4), [Fe(8)O(3)(Me-sao)(3)(tea)(teaH)(3)(O(2)CMe)(3)] (5), [Fe(8)O(3)(Et-sao)(3)(tea)(teaH)(3)(O(2)CMe)(3)] (6), and [Fe(8)O(3)(Ph-sao)(3)(tea)(teaH)(3)(O(2)CMe)(3)] (7) are reported (Me-saoH(2) is 2'-hydroxyacetophenone oxime, Et-saoH(2) is 2'-hydroxypropiophenone oxime and Ph-saoH(2) is 2-hydroxybenzophenone oxime). 1-7
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.
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
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