2-Hydroxyethyl phenoxyacetate

Base Information

• Chemical Name: 2-Hydroxyethyl phenoxyacetate
• CAS No.: 1984-60-7
• Molecular Formula: C10H12 O4
• Molecular Weight: 196.203
• Hs Code.: 2918990090
• European Community (EC) Number: 217-854-7
• DSSTox Substance ID: DTXSID6062096
• Nikkaji Number: J199.800E
• Wikidata: Q81989850
• Mol file: 1984-60-7.mol

Synonyms:2-Hydroxyethyl phenoxyacetate;2-hydroxyethyl 2-phenoxyacetate;1984-60-7;Acetic acid, phenoxy-, 2-hydroxyethyl ester;Acetic acid, 2-phenoxy-, 2-hydroxyethyl ester;EINECS 217-854-7;SCHEMBL1396715;2 - hydroxyethyl phenoxyacetate;DTXSID6062096;Mono Ethylene Glycol Phenoxy Acetate;Phenoxyacetic acid 2-hydroxyethyl ester

Chemical Property of 2-Hydroxyethyl phenoxyacetate

Chemical Property:

• Vapor Pressure: 2.19E-05mmHg at 25°C
• Boiling Point: 346.4°Cat760mmHg
• Flash Point: 137.2°C
• PSA: 55.76000
• Density: 1.196g/cm³
• LogP: 0.60090
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 196.07355886
• Heavy Atom Count: 14
• Complexity: 164

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)OCC(=O)OCCO

Technology Process of 2-Hydroxyethyl phenoxyacetate

There total 2 articles about 2-Hydroxyethyl phenoxyacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

ethylene glycol (107-21-1) + 2-phenoxyacetic acid (122-59-8) → 2′-hydroxy-1′-ethyl(2-phenoxy)acetate (1984-60-7)

Guidance literature:

With iodine; In toluene; Reflux;

DOI:10.1016/j.cclet.2015.04.008

Reference yield:

2-chloro-ethanol (107-07-3) → 2′-hydroxy-1′-ethyl(2-phenoxy)acetate (1984-60-7)

Guidance literature:

Reference yield:

(2-naphthoyl)oxyacetic acid (120-23-0) + 2′-hydroxy-1′-ethyl(2-phenoxy)acetate (1984-60-7) → 1-([2]naphthyloxy-acetoxy)-2-phenoxyacetoxy-ethane

Guidance literature:

With benzenesulfonic acid; at 140 ℃;

upstream raw materials:

ethylene glycol

2-phenoxyacetic acid

2-chloro-ethanol