152153
2-Formylphenoxyacetic acid
97%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
HCOC6H4OCH2CO2H
CAS Number:
Molecular Weight:
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).
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service