N,N,N-Trimethyl(phenylsulfanyl)methanaminium iodide

Base Information

Chemical Name:N,N,N-Trimethyl(phenylsulfanyl)methanaminium iodide
CAS No.:6631-73-8
Molecular Formula:C₁₀H₁₆NS*I
Molecular Weight:309.214
Hs Code.:
DSSTox Substance ID:DTXSID90492935
NSC Number:57923

Synonyms:6631-73-8;N,N,N-Trimethyl(phenylsulfanyl)methanaminium iodide;DTXSID90492935;NSC57923;NSC-57923

Suppliers and Price of N,N,N-Trimethyl(phenylsulfanyl)methanaminium 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 6 raw suppliers

Chemical Property of N,N,N-Trimethyl(phenylsulfanyl)methanaminium iodide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:309.00482
Heavy Atom Count:13
Complexity:122

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[N+](C)(C)CSC1=CC=CC=C1.[I-]

Technology Process of N,N,N-Trimethyl(phenylsulfanyl)methanaminium iodide

There total 3 articles about N,N,N-Trimethyl(phenylsulfanyl)methanaminium 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: 20.0%

: 43180-39-8
dimethyl<(phenylthio)methyl>amine

: 74-88-4
methyl iodide

: 6631-73-8
phenylthiomethyltrimethylammonium iodide

Guidance literature:: In acetonitrile; at 20 ℃; for 17h;
DOI:10.1021/jo000015f

Reference yield:

: 108-98-5
thiophenol

: 6631-73-8
phenylthiomethyltrimethylammonium iodide

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / H₂O / 20 - 80 °C

2: 20 percent / acetonitrile / 17 h / 20 °C

In water; acetonitrile; 1: Condensation / 2: Methylation;
DOI:10.1021/jo000015f

Reference yield:

: 108-98-5
thiophenol

: 6631-73-8
phenylthiomethyltrimethylammonium iodide

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous formaldehyde-solution

2: benzene

With formaldehyd; benzene;
DOI:10.1021/jo01357a616