All Photos(1)
About This Item
Linear Formula:
C6H5OCH2CO2C2H5
CAS Number:
Molecular Weight:
180.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
98%
refractive index
n20/D 1.505 (lit.)
bp
136 °C/19 mmHg (lit.)
density
1.1 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)COc1ccccc1
InChI
1S/C10H12O3/c1-2-12-10(11)8-13-9-6-4-3-5-7-9/h3-7H,2,8H2,1H3
InChI key
MGZFVSUXQXCEHM-UHFFFAOYSA-N
General description
Ethyl phenoxyacetate is an ester. It undergoes cyanide ion catalyzed aminolysis with ammonia to afford the corresponding amide.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis of Ethyl Phenoxyacetate Derivatives under Conditions of Phase-Transfer Catalysis and Ultrasonic Irradiation.
Kukovinets AG, et al.
Russ. J. Org. Chem., 34, 1331-1333 (1998)
Cyanide as an efficient and mild catalyst in the aminolysis of esters
Hogberg T, et al.
The Journal of Organic Chemistry, 52, 2033-2036 (1987)
Yongqiang Wu et al.
Luminescence : the journal of biological and chemical luminescence, 33(5), 855-862 (2018-04-18)
Six novel 8-hydroxyquinoline derivatives were synthesized using 2-methyl-8-hydroxyquinoline and para-substituted phenol as the main starting materials, and were characterized by 1 H nuclear magnetic resonance (NMR), mass spectrometry (MS), ultraviolet (UV) light analysis and infra-red (IR) light analysis. Their complexes
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service