158518
苯氧乙酸
98%
别名:
苯氧醋酸
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关于此项目
线性分子式:
C6H5OCH2CO2H
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-556-7
Beilstein/REAXYS Number:
907949
MDL number:
Assay:
98%
Form:
solid
InChI key
LCPDWSOZIOUXRV-UHFFFAOYSA-N
InChI
1S/C8H8O3/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)
SMILES string
OC(=O)COc1ccccc1
assay
98%
form
solid
mp
98-100 °C (lit.)
solubility
ethanol: soluble 10%, clear, colorless
Quality Level
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General description
苯氧乙酸是一种除草剂，并且已经研究了其以TiO2作为光催化剂的光降解作用。以1,2-二氯乙烷和Amberlite LA-2为载体的液膜研究了青霉素V与苯氧乙酸的选择性分离。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - 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
Rudina Bleta et al.
Langmuir : the ACS journal of surfaces and colloids, 30(39), 11812-11822 (2014-09-16)
A series of mesoporous titania photocatalysts with tailorable structural and textural characteristics was prepared in aqueous phase via a colloidal self-assembly approach using various cyclodextrins (CDs) as structure-directing agents. The photocatalysts and the structure-directing agents were characterized at different stages
Photocatalyzed Degradation of Phenol, 2, 4-Dichlorophenol, Phenoxyacetic Acid and 2, 4-Dichlorophenoxyacetic Acid over SupportedTiO2 in a Flow System.
Trillas M, et al.
Journal of Chemical Technology and Biotechnology, 67(3), 237-242 (1996)
Selective separation of penicillin V from phenoxyacetic acid using liquid membranes.
Cascaval D, et al.
Biochemical Engineering Journal, 55(1), 45-50 (2000)
Discovery of carboranes as inducers of 20S proteasome activity.
Hyun Seung Ban et al.
ChemMedChem, 5(8), 1236-1241 (2010-05-13)
Mohamed Ashraf Ali et al.
Bioorganic & medicinal chemistry, 15(5), 1896-1902 (2007-01-26)
A series of 2-{4-[1-amino (thioxo) methyl-5-(substituted phenyl)-4,5-dihydro-1H-3-pyrazolyl]-2-methoxyphenoxy}acetic acid and 2-{4-[1-carbamoyl-5-(substituted phenyl)-4,5-dihydro-1H-3-pyrazolyl]-2-methoxyphenoxy}acetic acid were synthesized and the in vitro activity of the synthesized compounds against Mycobacterium tuberculosis H37Rv (MTB) and INH-resistant M. tuberculosis (INHR-MTB) was studied. Among the synthesized compounds, compound
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