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About This Item
Linear Formula:
HOC6H4CONHOH
CAS Number:
Molecular Weight:
153.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-934-3
MDL number:
Assay:
99%
InChI
1S/C7H7NO3/c9-6-4-2-1-3-5(6)7(10)8-11/h1-4,9,11H,(H,8,10)
InChI key
HBROZNQEVUILML-UHFFFAOYSA-N
SMILES string
ONC(=O)c1ccccc1O
assay
99%
mp
177 °C (dec.) (lit.)
Quality Level
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Application
Salicylhydroxamic acid can be used:
- To prepare phenylboronic acid-based bioconjugates for chromatographic applications.
- As a ligand to synthesize Fe(III), Cu(II), Ni(II) and Zn(II) complexes.
- As a selective collector in the segregation of oxide minerals using the flotation method.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Carc. 2 - 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
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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A visualization method for studying the adsorption of lead species in salicylhydroxamic acid flotation of hemimorphite
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Ascochyta blight (AB) of pulse crops (chickpea, field pea, and lentils) causes yield loss in Montana, where 1.2 million acres was planted to pulses in 2016. Pyraclostrobin and azoxystrobin, quinone outside inhibitor (QoI) fungicides, have been the choice of farmers
Metal complexes of salicylhydroxamic acid (H2Sha), anthranilic hydroxamic acid and benzohydroxamic acid. Crystal and molecular structure of [Cu (phen) 2 (Cl)] Cl . H2Sha, a model for a peroxidase-inhibitor complex
O'Brien EC, et al.
Journal of Inorganic Biochemistry, 79(1-4), 47-51 (2000)
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