(3-Fluorophenyl)methanesulfonamide

Base Information

Chemical Name:(3-Fluorophenyl)methanesulfonamide
CAS No.:919353-99-4
Molecular Formula:C7H8FNO2S
Molecular Weight:189.21
Hs Code.:
European Community (EC) Number:843-260-8
DSSTox Substance ID:DTXSID60655651
Wikidata:Q82569861

Synonyms:(3-fluorophenyl)methanesulfonamide;919353-99-4;Benzenemethanesulfonamide, 3-fluoro-;1-(3-fluorophenyl)methanesulfonamide;SCHEMBL3218746;DTXSID60655651;GMGURIXOPQPLIV-UHFFFAOYSA-N;AKOS009343385;AM101594;CS-0233505;EN300-134058;Z385450912

Suppliers and Price of (3-Fluorophenyl)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 3 raw suppliers

Chemical Property of (3-Fluorophenyl)methanesulfonamide

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:189.02597783
Heavy Atom Count:12
Complexity:234

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)F)CS(=O)(=O)N

Technology Process of (3-Fluorophenyl)methanesulfonamide

There total 4 articles about (3-Fluorophenyl)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: 100.0%

: 919353-99-4
1-(3-fluorophenyl)methanesulfonamide

Guidance literature:

Reference yield: 74.0%

: 24974-72-9
(3-fluorophenyl)methanesulphonyl chloride

: 919353-99-4
1-(3-fluorophenyl)methanesulfonamide

Guidance literature:: With ammonium hydroxide; In methanol; at 20 ℃; for 3h;

Reference yield:

: 456-42-8
m-fluorobenzyl chloride

: 919353-99-4
1-(3-fluorophenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 1 h / Reflux

2: hydrogenchloride; N-chloro-succinimide / acetonitrile / 0.33 h / 10 - 20 °C

3: ammonium hydroxide; ammonium carbonate / tetrahydrofuran / 1 h / 20 °C

With hydrogenchloride; ammonium hydroxide; N-chloro-succinimide; ammonium carbonate; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1021/acs.jmedchem.8b01971