N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzenesulfonamide

Base Information

Chemical Name:N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzenesulfonamide
CAS No.:716375-92-7
Molecular Formula:C₁₅H₁₄N₂O₃S₂
Molecular Weight:334.42
Hs Code.:
ChEMBL ID:CHEMBL1339149
DSSTox Substance ID:DTXSID101324882
Pharos Ligand ID:43LAJJ3M8MAX
Wikidata:Q27164871

Synonyms:N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzenesulfonamide;716375-92-7;MLS000773738;MLS003116069;KUC104125N;SMR000364449;N,N-Dimethyl-3-(3-oxobenzo[d]isothiazol-2(3H)-yl)benzenesulfonamide;MLS002460504;CHEMBL1339149;BDBM34966;CHEBI:93150;cid_5040456;DTXSID101324882;HMS2218K20;HMS3340G17;EX-A5608;AKOS034456038;KSC-09-049;MLS 0263839?;VU0316361-2;MLS-0263839.0001;MLS-0263839.0002;MLS-0263839.0003;EN300-26868407;Q27164871;Z56798522;3-(3-keto-1,2-benzothiazol-2-yl)-N,N-dimethyl-benzenesulfonamide;N,N-dimethyl-3-(3-oxidanylidene-1,2-benzothiazol-2-yl)benzenesulfonamide;N,N-dimethyl-3-(3-oxo-2,3-dihydro-1,2-benzothiazol-2-yl)benzene-1-sulfonamide

Suppliers and Price of N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzenesulfonamide

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,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzenesulfonamide

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:334.04458466
Heavy Atom Count:22
Complexity:529

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN(C)S(=O)(=O)C1=CC=CC(=C1)N2C(=O)C3=CC=CC=C3S2

Technology Process of N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzenesulfonamide

There total 2 articles about N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzenesulfonamide 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:

: 1622393-02-5
C₁₅H₁₆N₂O₃S₂

: 716375-92-7
C₁₅H₁₄N₂O₃S₂

Guidance literature:: With trifluoroacetic acid; bis-[(trifluoroacetoxy)iodo]benzene; In dichloromethane; at 20 ℃;
DOI:10.1016/j.bmcl.2014.07.013

Reference yield:

: 6274-18-6
3-amino-N,N-dimethylbenzenesulfonamide

: 4892-02-8
Methyl thiosalicylate

: 716375-92-7
C₁₅H₁₄N₂O₃S₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: trimethylaluminum / dichloromethane; tetrahydrofuran / 0.5 h / 0 - 20 °C / Inert atmosphere

1.2: 60 °C / Inert atmosphere

2.1: bis-[(trifluoroacetoxy)iodo]benzene; trifluoroacetic acid / dichloromethane / 20 °C

With trimethylaluminum; trifluoroacetic acid; bis-[(trifluoroacetoxy)iodo]benzene; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2014.07.013