12-(p-Iodophenyl)dodecanol

Base Information

Chemical Name:12-(p-Iodophenyl)dodecanol
CAS No.:167634-94-8
Molecular Formula:C18H29IO
Molecular Weight:388.332
Hs Code.:
DSSTox Substance ID:DTXSID10471121
Mol file:167634-94-8.mol

Synonyms:12-(p-Iodophenyl)dodecanol;Benzenedodecanol, 4-iodo-;167634-94-8;SCHEMBL1263897;DTXSID10471121;BPIAUJNGDUSASC-UHFFFAOYSA-N

Suppliers and Price of 12-(p-Iodophenyl)dodecanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 12-(p-Iodophenyl)dodecanol

Chemical Property:

XLogP3:7.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:12
Exact Mass:388.12631
Heavy Atom Count:20
Complexity:200

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CCCCCCCCCCCCO)I

Technology Process of 12-(p-Iodophenyl)dodecanol

There total 7 articles about 12-(p-Iodophenyl)dodecanol 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: 90.0%

: 873301-56-5
tetrahydro-2-[12-(p-iodophenyl)dodecyloxy]-2H-pyran

: 167634-94-8
12-(p-iodophenyl)dodecanol

Guidance literature:: With ethanol; pyridinium p-toluenesulfonate; at 50 ℃; for 3h;
DOI:10.1021/jm050252g

Reference yield: 87.0%

: 1092072-76-8
12-(p-iodophenyl)dodecyl acetate

: 167634-94-8
12-(p-iodophenyl)dodecanol

Guidance literature:: 12-(p-iodophenyl)dodecyl acetate; With sodium hydroxide; water; In tetrahydrofuran; methanol; at 20 ℃; for 5h;

With hydrogenchloride; In tetrahydrofuran; methanol; water; pH=7;

Reference yield:

: 16004-15-2
1-bromomethyl-4-iodobenzene

: 167634-94-8
12-(p-iodophenyl)dodecanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: Mg / tetrahydrofuran / 20 °C

1.2: Li₂CuCl₄ / tetrahydrofuran / -78 °C

1.3: 55 percent / tetrahydrofuran / 17 h / -78 - 20 °C

2.1: 90 percent / pyridinium p-toluenesulfonate; ethanol / 3 h / 50 °C

With ethanol; pyridinium p-toluenesulfonate; magnesium; In tetrahydrofuran;
DOI:10.1021/jm050252g