N,N-dimethylbenzenesulfonoimidamide

Base Information

Chemical Name:N,N-dimethylbenzenesulfonoimidamide
CAS No.:69726-86-9
Molecular Formula:C₈H₁₂N₂OS
Molecular Weight:184.262
Hs Code.:
European Community (EC) Number:848-143-5

Synonyms:N,N-dimethylbenzenesulfonoimidamide;69726-86-9;N-methyl-N-(phenylsulfonimidoyl)methanamine;EN300-260688

Suppliers and Price of N,N-dimethylbenzenesulfonoimidamide

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 2 raw suppliers

Chemical Property of N,N-dimethylbenzenesulfonoimidamide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:184.06703418
Heavy Atom Count:12
Complexity:237

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN(C)S(=N)(=O)C1=CC=CC=C1

Technology Process of N,N-dimethylbenzenesulfonoimidamide

There total 5 articles about N,N-dimethylbenzenesulfonoimidamide 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: 72.0%

: 5539-54-8
N,N-dimethylbenzenesulfinamide

: 69726-86-9
N,N-dimethylbenzenesulfonimidoamide

Guidance literature:: With [bis(acetoxy)iodo]benzene; ammonium carbamate; In methanol; at 25 ℃;
DOI:10.1002/chem.201703272

Reference yield:

: 108-98-5
thiophenol

: 69726-86-9
N,N-dimethylbenzenesulfonimidoamide

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuryl dichloride; acetic acid / 3.5 h / -40 - 25 °C

2: dichloromethane / -40 - 25 °C

3: ammonium carbamate; [bis(acetoxy)iodo]benzene / methanol / 25 °C

With sulfuryl dichloride; [bis(acetoxy)iodo]benzene; ammonium carbamate; acetic acid; In methanol; dichloromethane;
DOI:10.1002/chem.201703272

Reference yield:

: 4972-29-6
benzenesulphinyl chloride

: 69726-86-9
N,N-dimethylbenzenesulfonimidoamide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / -40 - 25 °C

2: ammonium carbamate; [bis(acetoxy)iodo]benzene / methanol / 25 °C

With [bis(acetoxy)iodo]benzene; ammonium carbamate; In methanol; dichloromethane;
DOI:10.1002/chem.201703272