3540-90-7

Basic information

• Product Name: (1Z)-1,2-diphenylethane-1,2-dione semicarbazone
• CAS NO: 3540-90-7
• Molecular Formula: C₁₅H₁₃N₃O₂
• Molecular Weight: 267.2826
• Mol File: 3540-90-7.mol
• Article Data: 2

Chemical Properties

• Density: 1.22g/cm³
• Refractive Index: 1.617
• CAS DataBase Reference: (1Z)-1,2-diphenylethane-1,2-dione semicarbazone(CAS DataBase Reference)
• NIST Chemistry Reference: (1Z)-1,2-diphenylethane-1,2-dione semicarbazone(3540-90-7)
• EPA Substance Registry System: (1Z)-1,2-diphenylethane-1,2-dione semicarbazone(3540-90-7)

Safety Data

• Hazardous Substances Data: 3540-90-7(Hazardous Substances Data)

Usage

General Description

"(1Z)-1,2-diphenylethane-1,2-dione semicarbazone" is a chemical compound consisting of a semicarbazone group attached to a 1,2-diphenylethane-1,2-dione moiety. It is commonly used as a reagent in organic synthesis and can be used to detect and quantify certain functional groups in compounds. (1Z)-1,2-diphenylethane-1,2-dione semicarbazone has been studied for its potential biological activities and has been found to exhibit antiviral, antibacterial, and antifungal properties. Additionally, it has shown potential as an anti-inflammatory agent. (1Z)-1,2-diphenylethane-1,2-dione semicarbazone has also been investigated for its potential as a chelating agent in analytical chemistry. Overall, this compound has a diverse range of potential applications in various scientific and industrial fields.

Upstream product

• 563-41-7 semicarbazide hydrochloride 
• 134-81-6 benzil 
• 4426-72-6 hydrazine carboxamide 

Downstream Products

• 31283-03-1 6-methoxy-1,6-diphenyl-4-oxo-3,4,5,6-tetrahydro-2,3,5-triazine 
• 4512-00-9 5,6-diphenyl-1,2,4-triazin-3(2H)-one 
• 33668-66-5 1,2-Diphenyl-2-semicarbazido-aethan-1-on 
• 109450-14-8 2-hydroxy-1,2-diphenyl-propan-1-one semicarbazone 
• 109400-63-7 2-hydroxy-1,2-diphenyl-butan-1-one semicarbazone 
• 119077-40-6 2-hydroxy-2-[1]naphthyl-1,2-diphenyl-ethanone semicarbazone 
• 4512-00-9 5,6-diphenyl-1,2,4-triazin-3-one 

Relevant articles and documents

Selective access to new semicarbazones and thiosemicarbazones derived from benzil. Study of their conversion reactions

New Schiff bases from benzil with semicarbazide and thiosemicarbazide are reported. An open chain molecule, benzilbissemicarbazone 1 was prepared in presence of lithium hydroxide. A cycle 6-methoxy-1,6-diphenyl-4-thio- 3,4,5,6-tetrahydro-2,3,5-triazine 7 was obtained from thiosemicarbazide. A cyclic molecule, 1,6-diphenyl-4-oxo-3,4,5,6-tetrahydro-2,3,5-triazine 4 was produced from the recrystallization of 3 in chloroform. A new macrocyclic complex 8 was isolated from the open chain 6 in the presence of iron (III) chloride hexahydrated. Compounds 1, 2 convert into the cyclic 3 heated under reflux. In addition, we have got an iron complex 5 of 1 using the compound 2 as precursor. The crystal structure of 7 was obtained by single crystal X- Ray diffraction.