Diethyl 5-[[2-[[5-(2,6-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetyl]amino]-3-methylthiophene-2,4-dicarboxylate

Base Information

Chemical Name:Diethyl 5-[[2-[[5-(2,6-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetyl]amino]-3-methylthiophene-2,4-dicarboxylate
CAS No.:6241-45-8
Molecular Formula:C32H26 Cl2 N4 O4
Molecular Weight:535.5899
Hs Code.:
DSSTox Substance ID:DTXSID00411177
Wikidata:Q82217712

Synonyms:6241-45-8;diethyl 5-[[2-[[5-(2,6-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetyl]amino]-3-methylthiophene-2,4-dicarboxylate;DTXSID00411177

Suppliers and Price of Diethyl 5-[[2-[[5-(2,6-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetyl]amino]-3-methylthiophene-2,4-dicarboxylate

Supply Marketing:

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

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Chemical Property of Diethyl 5-[[2-[[5-(2,6-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetyl]amino]-3-methylthiophene-2,4-dicarboxylate

Chemical Property:

Density:1.4g/cm³
XLogP3:4.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:13
Exact Mass:535.10830711
Heavy Atom Count:36
Complexity:751

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=C(SC(=C1C)C(=O)OCC)NC(=O)CSC2=NN=C(O2)C3=C(C=CC=C3OC)OC

Technology Process of Diethyl 5-[[2-[[5-(2,6-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetyl]amino]-3-methylthiophene-2,4-dicarboxylate

There total 3 articles about Diethyl 5-[[2-[[5-(2,6-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetyl]amino]-3-methylthiophene-2,4-dicarboxylate 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: 35.0%

: 81-30-1
1,4,5,8-naphthalenetetracarboxylic dianhydride

: 6241-46-9
N¹-(2-chlorobenzyl)ethane-1,2-diamine

: 6241-45-8
2,7-bis-[2-(2-chlorobenzylamino)ethyl]benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone

Guidance literature:: In isopropyl alcohol; for 2h; Reflux;
DOI:10.1016/j.ejmech.2012.06.045

Reference yield:

: 89-98-5
2-chloro-benzaldehyde

: 6241-45-8
2,7-bis-[2-(2-chlorobenzylamino)ethyl]benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone

Guidance literature:: Multi-step reaction with 2 steps

1.1: toluene / 5 h / Reflux; Dean-Stark

1.2: 4 h / 0 - 20 °C

2.1: isopropyl alcohol / 2 h / Reflux

In isopropyl alcohol; toluene;
DOI:10.1016/j.ejmech.2012.06.045