alpha-Ethyl-3-hydroxy-2,4,6-triiodocinnamic acid

Base Information

Chemical Name:alpha-Ethyl-3-hydroxy-2,4,6-triiodocinnamic acid
CAS No.:1215-71-0
Molecular Formula:C₁₁H₉I₃O₃
Molecular Weight:569.904
Hs Code.:
Nikkaji Number:J106.764H
Wikidata:Q76325140
Mol file:1215-71-0.mol

Synonyms:BRN 2700104;alpha-Ethyl-3-hydroxy-2,4,6-triiodocinnamic acid;CINNAMIC ACID, alpha-ETHYL-3-HYDROXY-2,4,6-TRIIODO-;alpha-Aethyl-beta-(2,4,6-trijod-3-hydroxyphenyl)-acrylsaeure [German];alpha-Aethyl-beta-(2,4,6-trijod-3-hydroxyphenyl)-acrylsaeure;1215-71-0;C11H9I3O3;C11-H9-I3-O3;LS-54103;2-Ethyl-3-(3-hydroxy-2,4,6-triiodophenyl)propenoic acid

Suppliers and Price of alpha-Ethyl-3-hydroxy-2,4,6-triiodocinnamic acid

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 1 raw suppliers

Chemical Property of alpha-Ethyl-3-hydroxy-2,4,6-triiodocinnamic acid

Chemical Property:

Vapor Pressure:9.35E-10mmHg at 25°C
Boiling Point:473.1°C at 760 mmHg
Flash Point:239.9°C
Density:2.561g/cm³
XLogP3:4.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:569.7686
Heavy Atom Count:17
Complexity:319

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(=CC1=C(C(=C(C=C1I)I)O)I)C(=O)O
Isomeric SMILES:CC/C(=C\C1=C(C(=C(C=C1I)I)O)I)/C(=O)O

Technology Process of alpha-Ethyl-3-hydroxy-2,4,6-triiodocinnamic acid

There total 3 articles about alpha-Ethyl-3-hydroxy-2,4,6-triiodocinnamic acid 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:

: 99-61-6
3-nitro-benzaldehyde

: 1215-71-0
α-Ethyl-β-<2,4,6-triiod-3-hydroxy-phenyl>-acrylsaeure

Guidance literature:: Multi-step reaction with 4 steps

1: (nPrCO)2O

2: H₂ / Raney-Ni / methanol

3: (i) aq. NaNO₂, H₂SO₄, (ii) (heating)

4: ICl, NaOH / methanol

With butanoic acid anhydride; sodium hydroxide; hydrogen; Iodine monochloride; nickel; In methanol;

Reference yield:

: 59150-78-6
2-[(3-aminophenyl)methylene]butyric acid

: 1215-71-0
α-Ethyl-β-<2,4,6-triiod-3-hydroxy-phenyl>-acrylsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: (i) aq. NaNO₂, H₂SO₄, (ii) (heating)

2: ICl, NaOH / methanol

With sodium hydroxide; Iodine monochloride; In methanol;