4-(4-Methoxyphenylsulfanyl)benzoic acid

Base Information

Chemical Name:4-(4-Methoxyphenylsulfanyl)benzoic acid
CAS No.:252973-46-9
Molecular Formula:C14H12O3S
Molecular Weight:260.313
Hs Code.:
DSSTox Substance ID:DTXSID00461334
Nikkaji Number:J2.190.270E
Wikidata:Q82285626
Mol file:252973-46-9.mol

Synonyms:4-(4-methoxyphenyl)sulfanylbenzoic Acid;4-(4-methoxyphenylsulfanyl)benzoic acid;252973-46-9;Benzoic acid, 4-[(4-methoxyphenyl)thio]-;SCHEMBL6932815;DTXSID00461334;VEQLAPRSSMRJRW-UHFFFAOYSA-N;AKOS011514492;4-[(4-methoxyphenyl) sulfanyl]benzoic acid;A1-05410

Suppliers and Price of 4-(4-Methoxyphenylsulfanyl)benzoic acid

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

Matrix Scientific
4-(4-Methoxyphenyl)sulfanylbenzoic acid 95%
2.500g
$ 1320.00

A1 Biochem Labs
4-(4-Methoxyphenyl)sulfanylbenzoicacid 95%
2.5 g
$ 800.00

Total 1 raw suppliers

Chemical Property of 4-(4-Methoxyphenylsulfanyl)benzoic acid

Chemical Property:

PSA：71.83000
LogP:3.54460
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:260.05071541
Heavy Atom Count:18
Complexity:266

Purity/Quality:: 4-(4-Methoxyphenyl)sulfanylbenzoic acid 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)SC2=CC=C(C=C2)C(=O)O

Technology Process of 4-(4-Methoxyphenylsulfanyl)benzoic acid

There total 2 articles about 4-(4-Methoxyphenylsulfanyl)benzoic acid 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%

: 696-63-9
4-Methoxybenzenethiol

: 619-58-9
4-iodobenzoic acid

: 252973-46-9
4-[(4-methoxyphenyl)thio]benzoic acid

Guidance literature:: 4-iodobenzoic acid; With dmap; SPPSLHMP SynPhase Lanterns(R); dacarbazine; In dichloromethane; N,N-dimethyl-formamide; at 50 ℃; for 15h;

4-Methoxybenzenethiol; With borohydride polymer supported Amberlite(R) IRA₄₀₀; bis(bipyridine)nickel(II) bromide; In tetrahydrofuran; ethanol; at 70 ℃; for 15h;

With trifluoroacetic acid; In dichloromethane;
DOI:10.1021/ol050939v

Reference yield: 90.0%

: 696-63-9
4-Methoxybenzenethiol

: 586-76-5
4-Bromobenzoic acid

: 252973-46-9
4-[(4-methoxyphenyl)thio]benzoic acid

Guidance literature:: 4-Bromobenzoic acid; With 1,2,3-Benzotriazole; copper(l) iodide; In dimethyl sulfoxide; for 0.166667h;

4-Methoxybenzenethiol; With caesium carbonate; In dimethyl sulfoxide; at 100 ℃; Further stages.;
DOI:10.1016/j.tetlet.2007.07.205

Reference yield: 85.7%

: 252973-46-9
4-[(4-methoxyphenyl)thio]benzoic acid

: 1571032-97-7,1571033-57-2
(Z)-N'-hydroxy-1-(3-(2-methoxyethoxy)benzyl)-6-oxo-1,6-dihydropyridine-3-carboximidamide

: 1571033-60-7
5-(5-(4-(4-methoxybenzylthio)phenyl)-1,2,4-oxadiazol-3-yl)-1-(3-(2-methoxyethoxy)benzyl)pyridin-2(1H)-one

Guidance literature:: With potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 110 ℃; for 16h;