152153
2-甲酰苯氧乙酸
97%
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关于此项目
线性分子式:
HCOC6H4OCH2CO2H
化学文摘社编号:
分子量:
180.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
228-480-9
MDL number:
Assay:
97%
Form:
solid
InChI key
ANWMNLAAFDCKMT-UHFFFAOYSA-N
InChI
1S/C9H8O4/c10-5-7-3-1-2-4-8(7)13-6-9(11)12/h1-5H,6H2,(H,11,12)
SMILES string
OC(=O)COc1ccccc1C=O
assay
97%
form
solid
mp
129.5-132 °C (lit.)
functional group
aldehyde, carboxylic acid
Application
2-Formylphenoxyacetic acid was used to synthesize azomethine derivatives. It was also used in the preparation of ligands L(1)H(2) and L(2)H(2).
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Priya P Netalkar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 762-770 (2012-08-21)
A series of novel Co(II), Ni(II), Cu(II) and Zn(II) complexes of tri and tetratopic hydrazones have been prepared. Ligands L(1)H(2) and L(2)H(2) were synthesized by the condensation of 2-formylphenoxyacetic acid with 2-hydrazinobenzothiazole and 2-hydroxy-3-hydrazinebenzopyrazine, respectively. The prepared complexes were characterized
Amjid Iqbal et al.
Molecules (Basel, Switzerland), 12(2), 245-254 (2007-09-12)
A series of eight new azomethine derivatives were synthesized by reacting 2-formylphenoxyacetic acid with aromatic amines. The chemical structures of these compounds were confirmed by means of 1H-NMR, 13C-NMR, MS and elemental analysis. The compounds were assayed by the disc
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