Phenyl 3-iodopropanoate

Base Information

Chemical Name:Phenyl 3-iodopropanoate
CAS No.:138174-08-0
Molecular Formula:C₉H₉IO₂
Molecular Weight:276.074
Hs Code.:
DSSTox Substance ID:DTXSID60562356
Nikkaji Number:J992.999A
Wikidata:Q82446472
Mol file:138174-08-0.mol

Synonyms:Phenyl 3-iodopropanoate;138174-08-0;DTXSID60562356

Suppliers and Price of Phenyl 3-iodopropanoate

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

Total 3 raw suppliers

Chemical Property of Phenyl 3-iodopropanoate

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:275.96473
Heavy Atom Count:12
Complexity:142

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC(=O)CCI

Technology Process of Phenyl 3-iodopropanoate

There total 1 articles about Phenyl 3-iodopropanoate 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:

: 116385-40-1
((Z)-3-Iodo-1-phenoxy-propenyloxy)-trimethyl-silane

: 138174-08-0
3-Iodo-propionic acid phenyl ester

Guidance literature:: With water;
DOI:10.1246/bcsj.64.2965

Reference yield:

: 5781-53-3
monomethyl oxalyl chloride

: 67-56-1
methanol

: 138174-08-0
3-Iodo-propionic acid phenyl ester

: succinic acid methyl ester phenyl ester

Guidance literature:: With bis(tri-n-butyltin); triethylamine; Yield given; Multistep reaction; 1.) benzene, irradiation, 20 h; 2.) benzene, CH₂Cl₂, 0 deg C then r.t., 30 min;
DOI:10.1016/S0040-4039(98)01568-8