4-(4-Aminophenyl)-1,2,4-triazolidine-3,5-dione

Base Information

Chemical Name:4-(4-Aminophenyl)-1,2,4-triazolidine-3,5-dione
CAS No.:140707-19-3
Molecular Formula:C8H8N4O2
Molecular Weight:192.177
Hs Code.:
DSSTox Substance ID:DTXSID50471382
Nikkaji Number:J1.503.201D

Synonyms:4-(4-aminophenyl)-1,2,4-triazolidine-3,5-dione;140707-19-3;SCHEMBL11876869;DTXSID50471382;MFCD09928736;AKOS000166969;AS-67771;EN300-70357;D85691

Suppliers and Price of 4-(4-Aminophenyl)-1,2,4-triazolidine-3,5-dione

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
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price

Total 1 raw suppliers

Chemical Property of 4-(4-Aminophenyl)-1,2,4-triazolidine-3,5-dione

Chemical Property:

PSA：97.19000
LogP:0.84190
XLogP3:0
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:192.06472551
Heavy Atom Count:14
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N)N2C(=O)NNC2=O

Technology Process of 4-(4-Aminophenyl)-1,2,4-triazolidine-3,5-dione

There total 7 articles about 4-(4-Aminophenyl)-1,2,4-triazolidine-3,5-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: 100.0%

: 410535-09-0
1-ethoxycarbonyl-4-(4-aminophenyl)semicarbazide

: 140707-19-3
4-(4-aminophenyl)-1,2,4-triazolidine-3,5-dione

Guidance literature:: With sodium ethanolate; In ethanol; for 4.5h; Heating;

Reference yield: 96.0%

: 13274-45-8
4-(p-nitrophenyl)urazole

: 140707-19-3
4-(4-aminophenyl)-1,2,4-triazolidine-3,5-dione

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃; for 24h;

Reference yield:

: 13274-47-0
N-{[(4-nitrophenyl)carbamoyl]amino}ethoxyformamide

: 140707-19-3
4-(4-aminophenyl)-1,2,4-triazolidine-3,5-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / SnCl₂*2H₂O / ethanol / 4.5 h / Heating

2: 100 percent / sodium ethoxide / ethanol / 4.5 h / Heating

With sodium ethanolate; tin(ll) chloride; In ethanol;