5-Chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-1H-indole-2-carboxamide

Base Information

Chemical Name:5-Chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-1H-indole-2-carboxamide
CAS No.:121650-04-2
Molecular Formula:C24H17 Cl N4 O2 S
Molecular Weight:460.9354
Hs Code.:
Mol file:121650-04-2.mol

Synonyms:BRN 4599494;1H-Indole-2-carboxamide, 5-chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-;5-Chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-1H-indole-2-carboxamide;121650-04-2;C24H17ClN4O2S;C24-H17-Cl-N4-O2-S;LS-82484

Suppliers and Price of 5-Chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-1H-indole-2-carboxamide

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 1 raw suppliers

Chemical Property of 5-Chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-1H-indole-2-carboxamide

Chemical Property:

Density:1.44g/cm³
XLogP3:6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:460.0760747
Heavy Atom Count:32
Complexity:738

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(=O)N(C(=NC2=CC=CC=C2)S1)NC(=O)C3=C(C4=C(N3)C=CC(=C4)Cl)C5=CC=CC=C5

Technology Process of 5-Chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-1H-indole-2-carboxamide

There total 4 articles about 5-Chloro-N-(4-oxo-2-(phenylimino)-3-thiazolidinyl)-3-phenyl-1H-indole-2-carboxamide 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: 79.0%

: 121649-92-1
1-phenyl-3-(5'-chloro-3'-phenyl-indole-2'-carboxamido)-thiourea

: 79-11-8
chloroacetic acid

: 121650-04-2
3-(5'-chloro-3'-phenyl-indole-2'-carboxamido)-2-phenylimino-4-thiazolidinone

Guidance literature:: With sodium acetate; In acetic acid; for 8h; Heating;

Reference yield:

: 25434-84-8
5-chloro-3-phenyl-1H-indole-2-carboxyhydrazide

: 121650-04-2
3-(5'-chloro-3'-phenyl-indole-2'-carboxamido)-2-phenylimino-4-thiazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / ethanol / 4 h / Heating

2: 79 percent / NaOAc / acetic acid / 8 h / Heating

With sodium acetate; In ethanol; acetic acid;

Reference yield:

: 103-72-0
phenyl isothiocyanate

: 121650-04-2
3-(5'-chloro-3'-phenyl-indole-2'-carboxamido)-2-phenylimino-4-thiazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / ethanol / 4 h / Heating

2: 79 percent / NaOAc / acetic acid / 8 h / Heating

With sodium acetate; In ethanol; acetic acid;