2-(1H-Indol-3-yl)-3-((4-methoxyphenyl)methyl)-4-thiazolidinone

Base Information

Chemical Name:2-(1H-Indol-3-yl)-3-((4-methoxyphenyl)methyl)-4-thiazolidinone
CAS No.:86427-43-2
Molecular Formula:C₁₉H₁₈N₂O₂S
Molecular Weight:338.43
Hs Code.:2934999090
DSSTox Substance ID:DTXSID401006833
Mol file:86427-43-2.mol

Synonyms:86427-43-2;BRN 4545163;2-(1H-Indol-3-yl)-3-((4-methoxyphenyl)methyl)-4-thiazolidinone;2-(1H-indol-3-yl)-3-[(4-methoxyphenyl)methyl]-1,3-thiazolidin-4-one;4-Thiazolidinone, 2-(1H-indol-3-yl)-3-((4-methoxyphenyl)methyl)-;2-(1H-INDOL-3-YL)-3-[(4-METHOXYPHENYL)METHYL]THIAZOLIDIN-4-ONE;2-(1H-indol-3-yl)-3-(4-methoxybenzyl)thiazolidin-4-one;DTXSID401006833;LS-151793

Suppliers and Price of 2-(1H-Indol-3-yl)-3-((4-methoxyphenyl)methyl)-4-thiazolidinone

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 4 raw suppliers

Chemical Property of 2-(1H-Indol-3-yl)-3-((4-methoxyphenyl)methyl)-4-thiazolidinone

Chemical Property:

Vapor Pressure:6.29E-16mmHg at 25°C
Boiling Point:633°C at 760 mmHg
Flash Point:336.6°C
PSA：70.63000
Density:1.328g/cm³
LogP:3.88860
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:338.10889899
Heavy Atom Count:24
Complexity:453

Purity/Quality:: 99.0% Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)CN2C(SCC2=O)C3=CNC4=CC=CC=C43

Technology Process of 2-(1H-Indol-3-yl)-3-((4-methoxyphenyl)methyl)-4-thiazolidinone

There total 3 articles about 2-(1H-Indol-3-yl)-3-((4-methoxyphenyl)methyl)-4-thiazolidinone 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: 70.0%

: 86427-28-3
3-indole

: 68-11-1
mercaptoacetic acid

: 86427-43-2
3-<3-(p-methoxybenzyl)-4-oxo-3-thiazolidinyl>indole

Guidance literature:: In benzene; Ambient temperature;

Reference yield:

: 487-89-8,1228547-52-1
Indole-3-carboxaldehyde

: 86427-43-2
3-<3-(p-methoxybenzyl)-4-oxo-3-thiazolidinyl>indole

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / glacial acetic acid / ethanol / 6 h / Heating

2: 70 percent / benzene / Ambient temperature

With acetic acid; In ethanol; benzene;

Reference yield:

: 2393-23-9
4-methoxy-benzylamine

: 86427-43-2
3-<3-(p-methoxybenzyl)-4-oxo-3-thiazolidinyl>indole

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / glacial acetic acid / ethanol / 6 h / Heating

2: 70 percent / benzene / Ambient temperature

With acetic acid; In ethanol; benzene;