Sodium ionophore IV

Base Information

Chemical Name:Sodium ionophore IV
CAS No.:172883-29-3
Molecular Formula:C₂₇H₄₆O₅
Molecular Weight:450.659
Hs Code.:
DSSTox Substance ID:DTXSID50401548
Nikkaji Number:J1.156.820C
Wikidata:Q82204714
Mol file:172883-29-3.mol

Synonyms:Sodium ionophore IV;172883-29-3;2,6,13,16,19-Pentaoxapentacyclo[18.4.4.47,12.01,20.07,12]dotriacontane;2,3:11,12-Didecalino-16-crown-5;SCHEMBL12414105;DTXSID50401548;AKOS025294716;J-010856;Sodium ionophore IV, Selectophore(TM), function tested

Suppliers and Price of Sodium ionophore IV

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

Sigma-Aldrich
Sodium ionophore IV Selectophore?, function tested
50mg
$ 514.00

Total 3 raw suppliers

Chemical Property of Sodium ionophore IV

Chemical Property:

Vapor Pressure:1.8E-13mmHg at 25°C
Boiling Point:594.4°C at 760 mmHg
Flash Point:231.8°C
PSA：46.15000
Density:1.1g/cm³
LogP:5.72430
Storage Temp.:2-8°C
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:0
Exact Mass:450.33452456
Heavy Atom Count:32
Complexity:531

Purity/Quality:

98%min ^*data from raw suppliers

Sodium ionophore IV Selectophore?, function tested ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC23CCCCC2(C1)OCCCOC45CCCCC4(CCCC5)OCCOCCO3

Technology Process of Sodium ionophore IV

There total 3 articles about Sodium ionophore IV 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:

: 28795-95-1
cis-9,10-decalinediol

: 172883-29-3
2,6,13,16,19-pentaoxapentacyclo<18.4.4.4^7,12.0^1,20.0^7,12>dotriacontane

Guidance literature:: Multi-step reaction with 3 steps

1: 51.4 percent / p-toluenesulfonic acid monohydrate / benzene / 2 h / 90 °C

2: 33.8 percent / lithium aluminum hydride, aluminum chloride / diethyl ether / 3 h

3: 1.) sodium hydride / 1.) THF, 40 deg C, 1 h, 2.) THF, 70 deg C, 20 h

With lithium aluminium tetrahydride; aluminium trichloride; sodium hydride; toluene-4-sulfonic acid; In diethyl ether; benzene;
DOI:10.1021/ac950773j

Reference yield:

: 12,12'-methylenedi-11,13-dioxatricyclo<4.4.3.0^1,6>tridecane

: 172883-29-3
2,6,13,16,19-pentaoxapentacyclo<18.4.4.4^7,12.0^1,20.0^7,12>dotriacontane

Guidance literature:: Multi-step reaction with 2 steps

1: 33.8 percent / lithium aluminum hydride, aluminum chloride / diethyl ether / 3 h

2: 1.) sodium hydride / 1.) THF, 40 deg C, 1 h, 2.) THF, 70 deg C, 20 h

With lithium aluminium tetrahydride; aluminium trichloride; sodium hydride; In diethyl ether;
DOI:10.1021/ac950773j

Reference yield:

: 34604-52-9
diethylene glycol dimesylate

: 259866-54-1
6,6'-(propylenedioxy)di-cis-1-hydroxybicyclo<4.4.0>decane

: 172883-29-3
2,6,13,16,19-pentaoxapentacyclo<18.4.4.4^7,12.0^1,20.0^7,12>dotriacontane

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1.) THF, 40 deg C, 1 h, 2.) THF, 70 deg C, 20 h;
DOI:10.1021/ac950773j