5-[(4-Phenoxyphenyl)methyl]-1,3-thiazolidine-2,4-dione

Base Information

Chemical Name:5-[(4-Phenoxyphenyl)methyl]-1,3-thiazolidine-2,4-dione
CAS No.:85002-17-1
Molecular Formula:C16H13NO3S
Molecular Weight:299.35
Hs Code.:
ChEMBL ID:CHEMBL611065
DSSTox Substance ID:DTXSID20510979

Synonyms:85002-17-1;5-[(4-Phenoxyphenyl)methyl]-1,3-thiazolidine-2,4-dione;DTXSID20510979

Suppliers and Price of 5-[(4-Phenoxyphenyl)methyl]-1,3-thiazolidine-2,4-dione

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 5-[(4-Phenoxyphenyl)methyl]-1,3-thiazolidine-2,4-dione

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:299.06161445
Heavy Atom Count:21
Complexity:387

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC2=CC=C(C=C2)CC3C(=O)NC(=O)S3

Technology Process of 5-[(4-Phenoxyphenyl)methyl]-1,3-thiazolidine-2,4-dione

There total 2 articles about 5-[(4-Phenoxyphenyl)methyl]-1,3-thiazolidine-2,4-dione 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: 42.0%

: 438190-31-9
5-(4-Phenoxy-benzylidene)-thiazolidine-2,4-dione

: 85002-17-1
5-(4-Phenoxy-benzyl)-thiazolidine-2,4-dione

Guidance literature:: With pyridine; lithium borohydride; In tetrahydrofuran; at 120 ℃; microwave irradiation;
DOI:10.1016/j.bmc.2005.08.056

Reference yield:

: 17356-08-0
thiourea

: 85002-17-1
5-(4-Phenoxy-benzyl)-thiazolidine-2,4-dione

Guidance literature:: With hydrogenchloride; Yield given. Multistep reaction; 1.) sulfolane, 120 deg C, 10 h; 2.) sulfolane, 100 deg C, 8 h;
DOI:10.1248/cpb.30.3580