393819
4-乙酰苯氧基乙酸
99%
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关于此项目
线性分子式:
CH3COC6H4OCH2CO2H
化学文摘社编号:
分子量:
194.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-524-2
MDL number:
Assay:
99%
InChI key
KMXZEXUYXUMHEQ-UHFFFAOYSA-N
InChI
1S/C10H10O4/c1-7(11)8-2-4-9(5-3-8)14-6-10(12)13/h2-5H,6H2,1H3,(H,12,13)
SMILES string
CC(=O)c1ccc(OCC(O)=O)cc1
assay
99%
mp
175-177 °C (dec.) (lit.)
solubility
methanol: soluble 25 mg/mL, clear, colorless to faintly yellow
functional group
carboxylic acid, ketone
General description
4-Acetylphenoxyacetic acid is a phenoxyacetic acid derivative. It has been synthesized by employing para-acetyl phenol as starting reagent.
Application
4-Acetylphenoxyacetic acid is suitable as a test compound in the study of phenylacetic acid transport system (PATS) of Pseudomonas putida U by the aerobic catabolism of phenylacetic acid derivative used as the sole carbon source.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
C Schleissner et al.
Journal of bacteriology, 176(24), 7667-7676 (1994-12-01)
The phenylacetic acid transport system (PATS) of Pseudomonas putida U was studied after this bacterium was cultured in a chemically defined medium containing phenylacetic acid (PA) as the sole carbon source. Kinetic measurement was carried out, in vivo, at 30
Design of new potent hypolipidemic agents with the synergistic structural properties of α-asarone and fibrates.
Zuniga C, et al.
Drug Development Research, 64(1), 28-40 (2005)
Photocyclization reactions. Part 1. Synthesis of dihydrobenzofuranols using photocyclization of 2-alkoxybenzaldehydes, 2'-alkoxyacetophenones, 2-formylphenoxyacetic acids and 2-acetylphenoxyacetic acids
Horaguchi T, et al.
Journal of Heterocyclic Chemistry, 28(5), 1261-1272 (1991)
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