1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion

Base Information

Chemical Name:1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion
CAS No.:96025-76-2
Molecular Formula:C₂₅H₂₁N₃O₃
Molecular Weight:411.46
Hs Code.:

1-(5-Ethoxy-5H-dibenzo<a,d>cyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion

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

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Chemical Property of 1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion

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Technology Process of 1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion

There total 4 articles about 1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion 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: 88.0%

: 64-17-5
ethanol

: 79536-76-8
2-(5H-Dibenzocyclohepten-5-ylio)-3,5-dioxo-4-phenyl-1,2,4-triazolidin-1-id

: 96025-76-2
1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion

Guidance literature:: In dichloromethane; for 0.25h; Ambient temperature;

Reference yield:

: 4233-33-4
4-Phenyl-1,2,4-triazolidine-3,5-dione

: 96025-76-2
1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / benzene / 5 h / Ambient temperature

2: 88 percent / CH₂Cl₂ / 0.25 h / Ambient temperature

In dichloromethane; benzene;

Reference yield:

: 6141-56-6
5-diazo-5H-dibenzocycloheptene

: 96025-76-2
1-(5-Ethoxy-5H-dibenzocyclohepten-5-yl)-4-phenyl-1,2,4-triazolidin-3,5-dion

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / benzene / 5 h / Ambient temperature

2: 88 percent / CH₂Cl₂ / 0.25 h / Ambient temperature

In dichloromethane; benzene;