4-Methoxybenzenesulfinamide

Base Information

Chemical Name:4-Methoxybenzenesulfinamide
CAS No.:61511-68-0
Molecular Formula:C7H9NO2S
Molecular Weight:171.22
Hs Code.:
DSSTox Substance ID:DTXSID10600530
Nikkaji Number:J270.109J

Synonyms:4-Methoxybenzenesulfinamide;61511-68-0;4-Methoxybenzene-1-sulfinamide;SCHEMBL10332481;DTXSID10600530

Suppliers and Price of 4-Methoxybenzenesulfinamide

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
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price

Total 0 raw suppliers

Chemical Property of 4-Methoxybenzenesulfinamide

Chemical Property:

PSA：71.53000
LogP:2.24250
XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:171.03539970
Heavy Atom Count:11
Complexity:143

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)S(=O)N

Technology Process of 4-Methoxybenzenesulfinamide

There total 4 articles about 4-Methoxybenzenesulfinamide 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: 82.0%

: 696-63-9
4-Methoxybenzenethiol

: 61511-68-0
(rac)-4-methoxybenzenesulfinamide

Guidance literature:: With methanol; [2,2]bipyridinyl; O-pivaloylhydroxylamine trifluoromethanesulfonate salt; iron(II) chloride; In dichloromethane; at 25 ℃; for 16h; Sealed tube;
DOI:10.1002/anie.202011138

Reference yield: 62.0%

: 31401-17-9
methyl p-methoxybenzenesulphinate

: 61511-68-0
(rac)-4-methoxybenzenesulfinamide

Guidance literature:: methyl p-methoxybenzenesulphinate; With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 - 20 ℃; for 2h;

With ammonium chloride; In tetrahydrofuran; for 1h;
DOI:10.1016/j.tetlet.2018.10.038