Iridomyrmecin

Base Information Edit

Chemical Name:Iridomyrmecin
CAS No.:485-43-8
Molecular Formula:C10H16O2
Molecular Weight:168.2328
Hs Code.:
UNII:9736R92EPU
DSSTox Substance ID:DTXSID40876125
Nikkaji Number:J6.000C
Wikipedia:Iridomyrmecin
Wikidata:Q2016116
Metabolomics Workbench ID:69310
Mol file:485-43-8.mol

Synonyms:iridomyrmecin

Suppliers and Price of Iridomyrmecin

Supply Marketing:Edit

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

American Custom Chemicals Corporation
IRIDOMYRMECIN 95.00%
5MG
$ 500.07

Total 5 raw suppliers

Chemical Property of Iridomyrmecin Edit

Chemical Property:

Vapor Pressure:0.0068mmHg at 25°C
Melting Point:60-61°
Refractive Index:nD65 1.4607
Boiling Point:270.5°Cat760mmHg
Flash Point:107.7°C
PSA：26.30000
Density:1g/cm³
LogP:1.84160
XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:168.115029749
Heavy Atom Count:12
Complexity:200

Purity/Quality:

99% ^*data from raw suppliers

IRIDOMYRMECIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC2C1COC(=O)C2C
Isomeric SMILES:C[C@H]1CC[C@H]2[C@@H]1COC(=O)[C@H]2C
Uses Iridomyrmecin (C10H16O2) is one of the few colorless compounds of iridium. It is used to manufacture insecticides. Insecticide, biocide.

Technology Process of Iridomyrmecin

There total 219 articles about Iridomyrmecin 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: 100.0%

: 60419-55-8
(+)-teucriumlactone

: 485-43-8,573-94-4,1127-68-0,1436-51-7,1436-62-0,2005-63-2,2005-70-1,2005-79-0,2567-37-5,16802-17-8,16802-18-9,26839-44-1,26839-45-2,26839-46-3,28021-46-7,72843-33-5,72843-34-6,107538-14-7,128657-97-6
iridomyrmecin

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol;

Reference yield: 100.0%

: 2-(2-(acetoxymethyl)-3-methylcyclopentyl)propanoic acid

: 485-43-8,573-94-4,1127-68-0,1436-51-7,1436-62-0,2005-63-2,2005-70-1,2005-79-0,2567-37-5,16802-17-8,16802-18-9,26839-44-1,26839-45-2,26839-46-3,28021-46-7,72843-33-5,72843-34-6,107538-14-7,128657-97-6
(+/-)-Isoiridomyrmecin

Guidance literature:: With toluene-4-sulfonic acid; In ethanol; at 60 ℃; for 36h;
DOI:10.1021/ol100077z

Reference yield: 96.0%

: C₁₀H₁₈O₂

: 485-43-8,573-94-4,1127-68-0,1436-51-7,1436-62-0,2005-63-2,2005-70-1,2005-79-0,2567-37-5,16802-17-8,16802-18-9,26839-44-1,26839-45-2,26839-46-3,28021-46-7,72843-33-5,72843-34-6,107538-14-7,128657-97-6
isoiridomyrmecin

Guidance literature:: With tetrapropylammonium perruthennate; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; at 20 ℃; for 3h; Solvent; Molecular sieve;