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

Base Information

Chemical Name:N-(3-phenylsulfanyl-4-pyridinyl)trifluoromethanesulfonamide
CAS No.:509076-59-9
Molecular Formula:C12H9F3N2O2S2
Molecular Weight:334.343
Hs Code.:
DSSTox Substance ID:DTXSID30458893
Wikidata:Q82282447
Pharos Ligand ID:PBF24N12KJK1
ChEMBL ID:CHEMBL224612

Synonyms:CHEMBL224612;N-(3-phenylsulfanyl-4-pyridinyl)trifluoromethanesulfonamide;509076-59-9;1,1,1-trifluoro-N-(3-phenylsulfanylpyridin-4-yl)methanesulfonamide;DTXSID30458893;ALOKHRRVYXMQQV-UHFFFAOYSA-N;BDBM50158437

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

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:334.00575437
Heavy Atom Count:21
Complexity:431

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)SC2=C(C=CN=C2)NS(=O)(=O)C(F)(F)F

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

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

: 509076-59-9
C,C,C-trifluoro-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

: 509076-59-9
C,C,C-trifluoro-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

: 509076-59-9
C,C,C-trifluoro-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