(2-Methyl-5-methylsulfanyl-oxazol-4-YL)triphenylphosphonium iodide

Base Information

Chemical Name:(2-Methyl-5-methylsulfanyl-oxazol-4-YL)triphenylphosphonium iodide
CAS No.:76621-78-8
Molecular Formula:C₂₃H₂₁NOPS*I
Molecular Weight:517.37
Hs Code.:
European Community (EC) Number:651-205-2
DSSTox Substance ID:DTXSID10589573

Synonyms:76621-78-8;(2-METHYL-5-METHYLSULFANYL-OXAZOL-4-YL)TRIPHENYLPHOSPHONIUM IODIDE;DTXSID10589573;[2-Methyl-5-(methylsulfanyl)-1,3-oxazol-4-yl](triphenyl)phosphanium iodide;AKOS016373443;(2-Methyl-5-(methylthio)oxazol-4-yl)triphenylphosphoniumiodide;(2-Methyl-5-(methylthio)oxazol-4-yl)triphenylphosphonium iodide;[2-METHYL-5-(METHYLSULFANYL)-1,3-OXAZOL-4-YL]TRIPHENYLPHOSPHANIUM IODIDE

Suppliers and Price of (2-Methyl-5-methylsulfanyl-oxazol-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

Total 3 raw suppliers

Chemical Property of (2-Methyl-5-methylsulfanyl-oxazol-4-YL)triphenylphosphonium iodide

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:517.01262
Heavy Atom Count:28
Complexity:412

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=NC(=C(O1)SC)[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[I-]

Technology Process of (2-Methyl-5-methylsulfanyl-oxazol-4-YL)triphenylphosphonium iodide

There total 2 articles about (2-Methyl-5-methylsulfanyl-oxazol-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: 50.0%

: 475198-55-1,76621-59-5,76621-93-7
(2-methyl-5-thioxo-2-oxazolin-4-ylidene)triphenylphosphorane

: 74-88-4
methyl iodide

: 76621-78-8
(2-Methyl-5-methylsulfanyl-oxazol-4-yl)-triphenyl-phosphonium; iodide

Guidance literature:: In methanol;

Reference yield:

: 76621-88-0
<1-(acetylamino)-2,2-dichlorovinyl>triphenylphosphonium chloride

: 76621-78-8
(2-Methyl-5-methylsulfanyl-oxazol-4-yl)-triphenyl-phosphonium; iodide

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / NaSH / methanol

2: 50 percent / methanol

With sodium hydrogensulfide; In methanol;