(4-Iodophenyl)methyl 1-methylheptyl carbonate

Base Information

Chemical Name:(4-Iodophenyl)methyl 1-methylheptyl carbonate
CAS No.:60075-73-2
Molecular Formula:C16H23IO3
Molecular Weight:390.2565
Hs Code.:
DSSTox Substance ID:DTXSID60975503

Synonyms:2-Octyl-p-iodobenzyl carbonate;(4-Iodophenyl)methyl 1-methylheptyl carbonate;BRN 1984876;Carbonic acid, (4-iodophenyl)methyl 1-methylheptyl ester;60075-73-2;(4-iodophenyl)methyl octan-2-yl carbonate;DTXSID60975503;LS-52070

Suppliers and Price of (4-Iodophenyl)methyl 1-methylheptyl carbonate

Supply Marketing:

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

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Chemical Property of (4-Iodophenyl)methyl 1-methylheptyl carbonate

Chemical Property:

Vapor Pressure:1.85E-06mmHg at 25°C
Boiling Point:395.4°Cat760mmHg
Flash Point:192.9°C
Density:1.361g/cm³
XLogP3:6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:10
Exact Mass:390.06919
Heavy Atom Count:20
Complexity:262

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(C)OC(=O)OCC1=CC=C(C=C1)I

Technology Process of (4-Iodophenyl)methyl 1-methylheptyl carbonate

There total 3 articles about (4-Iodophenyl)methyl 1-methylheptyl carbonate 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:

: 100-51-6,185532-71-2
benzyl alcohol

: 60075-73-2
Carbonic acid 4-iodo-benzyl ester 1-methyl-heptyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: (i) aq. NaIO₄, I₂, AcOH, H₂SO₄, (ii) KOH, MeOH

2: (i) toluene, (ii) /BRN= 1719322/, Py, CHCl₃

DOI:10.1021/jm00234a002