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Sigma-Aldrich

2-Formylphenoxyacetic acid

97%

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About This Item

Linear Formula:
HCOC6H4OCH2CO2H
CAS Number:
6280-80-4
Molecular Weight:
180.16
EC Number:
228-480-9
MDL number:
MFCD00003315
UNSPSC Code:
12352100
PubChem Substance ID:
24849206
NACRES:
NA.22
form:
solid
Assay:
97%

Assay

97%

form

solid

mp

129.5-132 °C (lit.)

functional group

aldehyde
carboxylic acid

SMILES string

OC(=O)COc1ccccc1C=O

InChI

1S/C9H8O4/c10-5-7-3-1-2-4-8(7)13-6-9(11)12/h1-5H,6H2,(H,11,12)

InChI key

ANWMNLAAFDCKMT-UHFFFAOYSA-N

Application

2-Formylphenoxyacetic acid was used to synthesize azomethine derivatives[1]. It was also used in the preparation of ligands L(1)H(2) and L(2)H(2)[2].

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ0475
MKBJ3190V
02917TH
16228HY
06223DY

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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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