(5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphonium iodide

Base Information

Chemical Name:(5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphonium iodide
CAS No.:76621-83-5
Molecular Formula:C₂₉H₂₅NPS₂*I
Molecular Weight:609.534
Hs Code.:2934100090
European Community (EC) Number:651-174-5
DSSTox Substance ID:DTXSID10383598

Synonyms:76621-83-5;(5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphonium iodide;(5-ethylsulfanyl-2-phenyl-1,3-thiazol-4-yl)-triphenylphosphanium;iodide;(5-ETHYLSULFANYL-2-PHENYL-THIAZOL-4-YL)TRIPHENYLPHOSPHONIUM IODIDE;DTXSID10383598;AKOS024318998;AG-H-05854;(5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphoniumiodide

Suppliers and Price of (5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphonium iodide

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
(5-ETHYLSULFANYL-2-PHENYL-THIAZOL-4-YL)-TRIPHENYL-PHOSPHONIUM, IODIDE AldrichCPR
1ea
$ 57.00

American Custom Chemicals Corporation
[5-(ETHYLTHIO)-2-PHENYL-1,3-THIAZOL-4-YL](TRIPHENYL)PHOSPHONIUM IODIDE 95.00%
25MG
$ 727.65

Total 0 raw suppliers

Chemical Property of (5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphonium iodide

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:609.02108
Heavy Atom Count:34
Complexity:531

Purity/Quality:: (5-ETHYLSULFANYL-2-PHENYL-THIAZOL-4-YL)-TRIPHENYL-PHOSPHONIUM, IODIDE AldrichCPR ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCSC1=C(N=C(S1)C2=CC=CC=C2)[P+](C3=CC=CC=C3)(C4=CC=CC=C4)C5=CC=CC=C5.[I-]

Technology Process of (5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphonium iodide

There total 3 articles about (5-(Ethylthio)-2-phenylthiazol-4-yl)triphenylphosphonium iodide 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: 90.0%

: 75-03-6
ethyl iodide

: 152877-46-8,76621-60-8,76621-94-8
(2-phenyl-5-thioxo-2-thiazolin-4-ylidene)triphenylphosphorane

: 76621-83-5
(5-Ethylsulfanyl-2-phenyl-thiazol-4-yl)-triphenyl-phosphonium; iodide

Guidance literature:: In methanol;

Reference yield:

: 55630-07-4
<1-(benzoylamino)-2,2-dichlorovinyl>triphenylphosphonium chloride

: 76621-83-5
(5-Ethylsulfanyl-2-phenyl-thiazol-4-yl)-triphenyl-phosphonium; iodide

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / PCl₅ / chlorobenzene / 12 h / 110 - 120 °C

2: 73 percent / NaSH / dimethylformamide; acetonitrile / 12 h / 20 - 25 °C

3: 90 percent / methanol

With sodium hydrogensulfide; phosphorus pentachloride; In methanol; N,N-dimethyl-formamide; chlorobenzene; acetonitrile;

Reference yield:

: 76621-72-2
<2,2-dichloro-1-<(α-chlorobenzylidene)amino>vinyl>triphenylphosphonium chloride

: 76621-83-5
(5-Ethylsulfanyl-2-phenyl-thiazol-4-yl)-triphenyl-phosphonium; iodide

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / NaSH / dimethylformamide; acetonitrile / 12 h / 20 - 25 °C

2: 90 percent / methanol

With sodium hydrogensulfide; In methanol; N,N-dimethyl-formamide; acetonitrile;