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2-Ethoxy-2-oxoethyl salicylate

Base Information
  • Chemical Name:2-Ethoxy-2-oxoethyl salicylate
  • CAS No.:27893-14-7
  • Molecular Formula:C11H12 O5
  • Molecular Weight:224.213
  • Hs Code.:2918230000
  • European Community (EC) Number:248-713-8
  • DSSTox Substance ID:DTXSID70182185
  • Nikkaji Number:J250.608D
  • Wikidata:Q83052836
  • Mol file:27893-14-7.mol
2-Ethoxy-2-oxoethyl salicylate

Synonyms:2-Ethoxy-2-oxoethyl salicylate;27893-14-7;EINECS 248-713-8;2-ethoxy-2-oxoethyl 2-hydroxybenzoate;SCHEMBL11409109;DTXSID70182185;STL561012;AKOS030507589;2-Hydroxybenzoic acid 2-ethoxy-2-oxoethyl ester

Suppliers and Price of 2-Ethoxy-2-oxoethyl salicylate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • (2-ETHOXY-2-OXOETHYL) 2-HYDROXYBENZOATE 95.00%
  • 5MG
  • $ 501.50
Total 5 raw suppliers
Chemical Property of 2-Ethoxy-2-oxoethyl salicylate
Chemical Property:
  • Vapor Pressure:3.4E-05mmHg at 25°C 
  • Boiling Point:344°Cat760mmHg 
  • PKA:7.89±0.30(Predicted) 
  • Flash Point:131.5°C 
  • PSA:72.83000 
  • Density:1.254g/cm3 
  • LogP:1.11210 
  • XLogP3:2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:224.06847348
  • Heavy Atom Count:16
  • Complexity:251
Purity/Quality:

99% *data from raw suppliers

(2-ETHOXY-2-OXOETHYL) 2-HYDROXYBENZOATE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)COC(=O)C1=CC=CC=C1O
Technology Process of 2-Ethoxy-2-oxoethyl salicylate

There total 3 articles about 2-Ethoxy-2-oxoethyl salicylate 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:
Guidance literature:
salicylic acid; With C28H35B9NiP2*CH2Cl2; In chloroform-d1; at 20 ℃; for 0.25h; Schlenk technique; Inert atmosphere;
diazoacetic acid ethyl ester; In chloroform-d1; at 35 ℃; regioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1002/chem.202005014
Guidance literature:
Natriumsalicylat, Aethoxychloracetat;
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