Chromoionophore X

Base Information

Chemical Name:Chromoionophore X
CAS No.:192190-92-4
Molecular Formula:C₃₂H₄₄F₃NO
Molecular Weight:515.703
Hs Code.:
DSSTox Substance ID:DTXSID30421744
Nikkaji Number:J898.590A
Wikidata:Q82233370
Mol file:192190-92-4.mol

Synonyms:Chromoionophore X;192190-92-4;1-[4-[(E)-2-[4-(dioctylamino)phenyl]ethenyl]phenyl]-2,2,2-trifluoroethanone;(E)-1-(4-(4-(Dioctylamino)styryl)phenyl)-2,2,2-trifluoroethan-1-one;SCHEMBL4695672;DTXSID30421744;LQCOAQAROPQVJL-FOCLMDBBSA-N;Chromoionophore X, Selectophore(TM);4-N,N-dioctylamino-4'-trifluoroacetylstilbene;alpha,alpha,alpha-Trifluoro-4'-[4-(dioctylamino)styryl]acetophenone

Suppliers and Price of Chromoionophore X

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
Chromoionophore X Selectophore
10mg
$ 121.00

Total 1 raw suppliers

Chemical Property of Chromoionophore X

Chemical Property:

PSA：20.31000
LogP:10.12940
XLogP3:11.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:18
Exact Mass:515.33749951
Heavy Atom Count:37
Complexity:600

Purity/Quality:: Chromoionophore X Selectophore ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCCCCCCCN(CCCCCCCC)C1=CC=C(C=C1)C=CC2=CC=C(C=C2)C(=O)C(F)(F)F
Isomeric SMILES:CCCCCCCCN(CCCCCCCC)C1=CC=C(C=C1)/C=C/C2=CC=C(C=C2)C(=O)C(F)(F)F

Technology Process of Chromoionophore X

There total 5 articles about Chromoionophore X 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:

: 2039-82-9
1-bromo-4-ethenyl-benzene

: 192190-92-4
1-{4-[(E)-2-(4-Dioctylamino-phenyl)-vinyl]-phenyl}-2,2,2-trifluoro-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: TEA

2: BuLi / tetrahydrofuran

With n-butyllithium; TEA; In tetrahydrofuran; 1: Substitution / 2: Acylation;
DOI:10.1039/a901961h

Reference yield:

: 111-83-1
1-bromo-octane

: 192190-92-4
1-{4-[(E)-2-(4-Dioctylamino-phenyl)-vinyl]-phenyl}-2,2,2-trifluoro-ethanone

Guidance literature:: Multi-step reaction with 3 steps

1: NEt(iPr)2 / dimethylformamide

2: TEA

3: BuLi / tetrahydrofuran

With n-butyllithium; TEA; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Substitution / 2: Substitution / 3: Acylation;
DOI:10.1039/a901961h

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 192190-92-4
1-{4-[(E)-2-(4-Dioctylamino-phenyl)-vinyl]-phenyl}-2,2,2-trifluoro-ethanone

Guidance literature:: Multi-step reaction with 3 steps

1: NEt(iPr)2 / dimethylformamide

2: TEA

3: BuLi / tetrahydrofuran

With n-butyllithium; TEA; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Substitution / 2: Substitution / 3: Acylation;
DOI:10.1039/a901961h