All Photos(2)
Linear Formula:
C2H5OC6H3-2-(OH)CHO
CAS Number:
Molecular Weight:
166.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
solid
bp
263-264 °C (lit.)
mp
66-68 °C (lit.)
SMILES string
CCOc1cccc(C=O)c1O
InChI
1S/C9H10O3/c1-2-12-8-5-3-4-7(6-10)9(8)11/h3-6,11H,2H2,1H3
InChI key
OFQBYHLLIJGMNP-UHFFFAOYSA-N
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Related Categories
Application
3-Ethoxysalicylaldehyde was used in the preparation of:
- Schiff base ligand via condensation with trans-1,2-diaminocyclohexane
- substituted salen-type Schiff base ligands
- a new Schiff base, 2-ethoxy-6-[(3-methylaminopropylimino)methyl]phenol, via reaction with N-methylpropane-1,3-diamine
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Synthesis, Crystal Structures, and Antibacterial Activities of Schiff-Base Zinc (II) Complexes [ZnL1Cl2] and [ZnL2I2]? 0.5 CH3OH.
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Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry, 41(8), 987-991 (2011)
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Inorganic chemistry, 49(19), 9012-9025 (2010-09-04)
Syntheses, characterization, and magnetic properties of a series of diphenoxo-bridged discrete dinuclear M(II)Ln(III) complexes (M = Cu or Ni, Ln = Ce-Yb) derived from the compartmental Schiff base ligand, H(2)L, obtained on condensation of 3-ethoxysalicylaldehyde with trans-1,2-diaminocyclohexane, are described. Single
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Hydroxylation of phenol catalyzed by oxovanadium (IV) of salen-type schiff base complexes with hydrogen peroxide.
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Catalysis Letters, 136(3-4), 228-233 (2010)
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Salophen (N,N'-bis-(salicylidene)-o-phenylenediamine) is a Schiff base, which is weakly emissive in solution, but strongly emissive in the solid state. The trend is reversed in its aluminium complex (SalAl
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