Ethane, 1-(2-iodoethoxy)-2-(2-methoxyethoxy)-

Base Information

• Chemical Name: Ethane, 1-(2-iodoethoxy)-2-(2-methoxyethoxy)-
• CAS No.: 62999-96-6
• Molecular Formula: C7H15IO3
• Molecular Weight: 274.099
• European Community (EC) Number: 886-773-2
• DSSTox Substance ID: DTXSID00442860
• Nikkaji Number: J2.883.562K
• Wikidata: Q82260410

Synonyms:62999-96-6;Ethane, 1-(2-iodoethoxy)-2-(2-methoxyethoxy)-;1-Iodo-3,6,9-trioxadecane;1-[2-(2-iodoethoxy)ethoxy]-2-methoxyethane;1-iodo-2-(2-(2-methoxyethoxy)ethoxy)ethane;1-IODO-2-[2-(2-METHOXYETHOXY)ETHOXY]ETHANE;SCHEMBL525968;DTXSID00442860;DLGFZOSPWIUMKY-UHFFFAOYSA-N;MFCD26911322;AKOS037649513;AT13074;BT-0159;{2-[2-(2-methoxyethoxy)ethoxy]ethyl}iodide;2-(2-Methoxyethoxy)ethyl 2-iodoethyl ether;1-iodo-2-[2-(2-methoxy-ethoxy)-ethoxy]-ethane;A917543

Chemical Property of Ethane, 1-(2-iodoethoxy)-2-(2-methoxyethoxy)-

Chemical Property:

• XLogP3: 0.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 274.00659
• Heavy Atom Count: 11
• Complexity: 70.7

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COCCOCCOCCI

Technology Process of Ethane, 1-(2-iodoethoxy)-2-(2-methoxyethoxy)-

There total 3 articles about Ethane, 1-(2-iodoethoxy)-2-(2-methoxyethoxy)- 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: 98.0%

2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate (62921-74-8,518012-62-9,58320-73-3) → 3,6,9-trioxadecyl iodide (62999-96-6)

Guidance literature:

With sodium iodide; In acetone; for 20h; Heating;

DOI:10.1021/jm070781f

Reference yield: 77.0%

triethylene glucol monomethyl ether (112-35-6,95507-80-5) → 3,6,9-trioxadecyl iodide (62999-96-6)

Guidance literature:

triethylene glucol monomethyl ether; With 1H-imidazole; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 0.05h; Inert atmosphere;

With iodine; In tetrahydrofuran; at 20 ℃; for 2h; Inert atmosphere;

DOI:10.1016/j.bioorg.2020.103849

Reference yield:

triethylene glucol monomethyl ether (112-35-6,95507-80-5) → 3,6,9-trioxadecyl iodide (62999-96-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 93 percent / pyridine / 6 h / 0 - 5 °C

2: 62 percent / NaI / acetone / 8 h / Heating

With pyridine; sodium iodide; In acetone;

DOI:10.1021/jo00129a045

upstream raw materials:

triethylene glucol monomethyl ether

2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate

Downstream raw materials:

C₃₄H₅₁N₂O₄⁽¹⁺⁾*I^(1-)

C₂₅H₃₃N₂O₄⁽¹⁺⁾*I^(1-)

C₂₀H₃₄BrNO₆

N-tosyl-2-[4-(ethylthio)-5-(2-(2-(2-methoxyethoxy)ethoxy)ethylthio)-(1,3)-dithiole-2-ylidene]-(1,3)-dithiolo[4,5-c]pyrrole

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