1,2,4-Triazolidine-3,5-dione, 4-phenyl-1-(2-propenyl)-

Base Information

• Chemical Name: 1,2,4-Triazolidine-3,5-dione, 4-phenyl-1-(2-propenyl)-
• CAS No.: 73970-92-0
• Molecular Formula: C11H11N3O2
• Molecular Weight: 217.227
• DSSTox Substance ID: DTXSID60434408
• Wikidata: Q82248823
• Mol file: 73970-92-0.mol

Synonyms:73970-92-0;1,2,4-Triazolidine-3,5-dione, 4-phenyl-1-(2-propenyl)-;DTXSID60434408

Chemical Property of 1,2,4-Triazolidine-3,5-dione, 4-phenyl-1-(2-propenyl)-

Chemical Property:

• XLogP3: 1.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 217.085126602
• Heavy Atom Count: 16
• Complexity: 310

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C=CCN1C(=O)N(C(=O)N1)C2=CC=CC=C2

Technology Process of 1,2,4-Triazolidine-3,5-dione, 4-phenyl-1-(2-propenyl)-

There total 7 articles about 1,2,4-Triazolidine-3,5-dione, 4-phenyl-1-(2-propenyl)- 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: 54.0%

4-Phenyl-1,2,4-triazolidine-3,5-dione (4233-33-4) + propene (187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4) → 1-(prop-enyl)-4-phenyl-1,2,4-triazolidine-3,5-dione (73970-92-0)

Guidance literature:

In dichloromethane; Ambient temperature; reaction with further ene comp.;

DOI:10.1021/jo01305a020

Reference yield:

4-Phenyl-1,2,4-triazolidine-3,5-dione (4233-33-4) + 1-<3-(Allyldimethylsilyl)prop-2-enyl>-4-methyl-1,2,4-triazoline-3,5-dione (75782-38-6) → C19H24N6O4Si (75790-44-2) + 1-(prop-enyl)-4-phenyl-1,2,4-triazolidine-3,5-dione (73970-92-0)

Guidance literature:

With methanol; Yield given. Multistep reaction; 1) acetonitrile, 2 h;

DOI:10.1021/jo00316a026

Reference yield:

4-Phenyl-1,2,4-triazolidine-3,5-dione (4233-33-4) + Allyltriphenylplumbane (38795-78-7) → 1-(prop-enyl)-4-phenyl-1,2,4-triazolidine-3,5-dione (73970-92-0)

Guidance literature:

With silica gel; Multistep reaction; 1.) chloroform, RT, 1 min, 2.) petr. ether, Et₂O;

upstream raw materials:

4-Phenyl-1,2,4-triazolidine-3,5-dione

propene

monoallyl(triphenyl)germane

allytriphenyltin

Downstream raw materials:

1-(2-propenyl)-2-methyl-4-phenyl-1,2,4-triazolidine-3,5-dione

1-glycidyl-2-acetyl-4-phenyl-1,2,3-triazolidine-3,5-dione

1-(2-propenyl)-2-acetyl-4-phenyl-1,2,4-triazolidine-3,5-dione

1-(2-Propenyl)-2-(trimethylsilyl)-4-phenyl-1,2,4-triazoline-3,5-dione