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462934

Sigma-Aldrich

Ethyl phenoxyacetate

98%

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About This Item

Linear Formula:
C6H5OCH2CO2C2H5
CAS Number:
2555-49-9
Molecular Weight:
180.20
EC Number:
219-867-3
MDL number:
MFCD00026895
UNSPSC Code:
12352100
PubChem Substance ID:
24870020
NACRES:
NA.22

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.[1]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

462934-VAR:
462934-BULK:
462934-100ML:
462934-25ML:

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Certificates of Analysis (COA)

Lot/Batch Number
33897LJ
12429MQ

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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)
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)
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

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