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Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester

Base Information Edit
  • Chemical Name:Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester
  • CAS No.:56703-36-7
  • Molecular Formula:C11H13IO3
  • Molecular Weight:320.127
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50434311
  • Nikkaji Number:J663.367F
  • Wikidata:Q82248681
  • Mol file:56703-36-7.mol
Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester

Synonyms:Ethyl 4-(2-iodoethoxy)benzoate;56703-36-7;Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester;SCHEMBL4518721;DTXSID50434311;4-(2-Iodoethoxy)benzoic acid ethyl ester;A1-05368

Suppliers and Price of Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester
Supply Marketing:Edit
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
  • Matrix Scientific
  • Ethyl 4-(2-iodoethoxy)benzoate 95%
  • 5g
  • $ 1403.00
  • A1 Biochem Labs
  • Ethyl4-(2-iodoethoxy)benzoate 95%
  • 5 g
  • $ 850.00
Total 0 raw suppliers
Chemical Property of Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester Edit
Chemical Property:
  • PSA:35.53000 
  • LogP:2.67710 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:6
  • Exact Mass:319.99094
  • Heavy Atom Count:15
  • Complexity:188
Purity/Quality:

Ethyl 4-(2-iodoethoxy)benzoate 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C1=CC=C(C=C1)OCCI
Technology Process of Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester

There total 7 articles about Benzoic acid, 4-(2-iodoethoxy)-, ethyl ester 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:
With sodium iodide; In acetone; for 12h; Yield given; Heating;
DOI:10.1248/cpb.43.829
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) NaH / 1.) THF, RT, 30 min, 2.) THF, RT, 1 h
2: 93 percent / 1N NaOH / ethanol / 3 h / Ambient temperature
3: 100 percent / NaBH4*Et2O / tetrahydrofuran / -78 - 20 °C
4: triethylamine / CH2Cl2 / 1 h / -78 °C
5: NaI / acetone / 12 h / Heating
With sodium hydroxide; sodium tetrahydroborate; diethyl ether; sodium hydride; triethylamine; sodium iodide; In tetrahydrofuran; ethanol; dichloromethane; acetone;
DOI:10.1248/cpb.43.829
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / NaBH4*Et2O / tetrahydrofuran / -78 - 20 °C
2: triethylamine / CH2Cl2 / 1 h / -78 °C
3: NaI / acetone / 12 h / Heating
With sodium tetrahydroborate; diethyl ether; triethylamine; sodium iodide; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1248/cpb.43.829
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