47743
4-Formylphenoxyacetic acid
≥97.0% (T)
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About This Item
Empirical Formula (Hill Notation):
C9H8O4
CAS Number:
Molecular Weight:
180.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
244-749-3
Beilstein/REAXYS Number:
779885
MDL number:
Product Name
4-Formylphenoxyacetic acid, ≥97.0% (T)
InChI key
OYNIIKHNXNPSAG-UHFFFAOYSA-N
InChI
1S/C9H8O4/c10-5-7-1-3-8(4-2-7)13-6-9(11)12/h1-5H,6H2,(H,11,12)
SMILES string
OC(=O)COc1ccc(C=O)cc1
assay
≥97.0% (T)
form
solid
mp
193-196 °C
storage temp.
2-8°C
Quality Level
General description
4-Formylphenoxyacetic acid is a formylphenoxyaliphatic acid that reacts with dimedone to form 1,8-dioxo-octahydroxanthenes. It participates in the synthesis of 4-substituted benzaldehyde derivatives and 4-carboxypheoxyacetic acid.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - 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
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Self-catalyzed syntheses, structural characterization, DPPH radical scavenging-, cytotoxicity-, and DFT studies of phenoxyaliphatic acids of 1, 8-dioxo-octahydroxanthene derivatives.
Kumar GSS, et al.
Journal of Molecular Structure, 1059, 51-60 (2014)
Synthesis of 2-, 3-and 4-Carboxyphenoxyacetic Acid: A Necessary Modi?cation.
Adak MM.
Asian Journal of Chemistry, 5(2), 464-466 (1993)
Wei Yi et al.
European journal of medicinal chemistry, 45(2), 639-646 (2009-11-26)
A series of novel 4-hydroxybenzaldehyde derivatives were synthesized and their inhibitory effects on the diphenolase activity of mushroom tyrosinase were investigated. Most of target compounds had more potent inhibitory activities than the parent compound 4-hydroxybenzaldehyde (IC(50)=1.22 mM). Interestingly, compound 3c
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