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Merck
CN

393819

Sigma-Aldrich

4-乙酰苯氧基乙酸

99%

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About This Item

线性分子式:
CH3COC6H4OCH2CO2H
CAS号:
分子量:
194.18
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

99%

mp

175-177 °C (dec.) (lit.)

溶解性

methanol: soluble 25 mg/mL, clear, colorless to faintly yellow

官能团

carboxylic acid
ketone

SMILES字符串

CC(=O)c1ccc(OCC(O)=O)cc1

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)

InChI key

KMXZEXUYXUMHEQ-UHFFFAOYSA-N

一般描述

4-Acetylphenoxyacetic acid is a phenoxyacetic acid derivative. It has been synthesized by employing para-acetyl phenol as starting reagent.

应用

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.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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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)
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)
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

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