N-(3-phenylsulfanyl-4-pyridinyl)methanesulfonamide

Base Information

Chemical Name:N-(3-phenylsulfanyl-4-pyridinyl)methanesulfonamide
CAS No.:833455-58-6
Molecular Formula:C12H12N2O2S2
Molecular Weight:280.371
Hs Code.:
ChEMBL ID:CHEMBL224122
DSSTox Substance ID:DTXSID10466638
Wikidata:Q82293234

Synonyms:CHEMBL224122;833455-58-6;N-(3-phenylsulfanyl-4-pyridinyl)methanesulfonamide;N-(3-phenylsulfanylpyridin-4-yl)methanesulfonamide;N-(3-(phenylthio)pyridin-4-yl)methanesulfonamide;DTXSID10466638;BDBM50158452;PD186819

Suppliers and Price of N-(3-phenylsulfanyl-4-pyridinyl)methanesulfonamide

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 1 raw suppliers

Chemical Property of N-(3-phenylsulfanyl-4-pyridinyl)methanesulfonamide

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:280.03401998
Heavy Atom Count:18
Complexity:348

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:CS(=O)(=O)NC1=C(C=NC=C1)SC2=CC=CC=C2

Technology Process of N-(3-phenylsulfanyl-4-pyridinyl)methanesulfonamide

There total 4 articles about N-(3-phenylsulfanyl-4-pyridinyl)methanesulfonamide 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:

: 13959-52-9
4-nitro-3-phenylsulfanylpyridine N-oxide

: 833455-58-6
N-(3-phenylsulfanyl-pyridin-4-yl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: Fe; aq. acetic acid / Heating

2: K₂CO₃ / acetonitrile

With iron; potassium carbonate; acetic acid; In acetonitrile;
DOI:10.1021/jm049480l

Reference yield:

: 1678-49-5
3-Bromo-4-nitropyridine N-oxide

: 833455-58-6
N-(3-phenylsulfanyl-pyridin-4-yl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / K₂CO₃ / toluene / 10 h / Heating

2: Fe; aq. acetic acid / Heating

3: K₂CO₃ / acetonitrile

With iron; potassium carbonate; acetic acid; In toluene; acetonitrile;
DOI:10.1021/jm049480l

Reference yield:

: 108-98-5
thiophenol

: 833455-58-6
N-(3-phenylsulfanyl-pyridin-4-yl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / K₂CO₃ / toluene / 10 h / Heating

2: Fe; aq. acetic acid / Heating

3: K₂CO₃ / acetonitrile

With iron; potassium carbonate; acetic acid; In toluene; acetonitrile;
DOI:10.1021/jm049480l