1425088-81-8

Basic information

• Product Name: 2-(5H-dibenzo[a,d][7]annulen-5-ylacetyl)-N-(4-ethylphenyl)hydrazinecarbothioamides
• CAS NO: 1425088-81-8
• Molecular Weight: 427.57
• Mol File: 1425088-81-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(5H-dibenzo[a,d][7]annulen-5-ylacetyl)-N-(4-ethylphenyl)hydrazinecarbothioamides(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5H-dibenzo[a,d][7]annulen-5-ylacetyl)-N-(4-ethylphenyl)hydrazinecarbothioamides(1425088-81-8)
• EPA Substance Registry System: 2-(5H-dibenzo[a,d][7]annulen-5-ylacetyl)-N-(4-ethylphenyl)hydrazinecarbothioamides(1425088-81-8)

Safety Data

• Hazardous Substances Data: 1425088-81-8(Hazardous Substances Data)

Upstream product

• 24330-10-7 ethyl 5H-dibenzo[a,d][7]annulen-5-ylacetate 
• 18856-63-8 (4-ethylphenyl)isothiocyanate 
• 947233-55-8 2-(5H-dibenzo[a,d][7]annulen-5-yl)acetohydrazide 
• 1643-43-2 5H-dibenzo[a,d]-cycloheptene-5-acetic acid 

Downstream Products

• 1425088-85-2 C₂₆H₂₃N₃S 

Relevant articles and documents

Synthesis and root growth activity of some new acetylhydrazinecarbothioamides and 1,2,4-triazoles substituted with the 5H-dibenzo[a,d][7]annulene moiety

New hydrazinecarbothioamides 5a-d bearing 5H-dibenzo[a,d][7]annulene moiety were synthesized using classical procedures. 1H-NMR analysis indicated the existence of two conformational isomers, a major axial (about 75 %) and a minor equatorial one (25 %), which are interconvertible by middle ring inversion. Cyclization of compounds 5a-d in NaOH solution produced the corresponding 4H-1,2,4-triazole-3-thiols (6a-d) that proved to be pure axial isomers. All the new compounds were extensively characterized by elemental analysis, IR, UV, 1H-NMR and 13C-NMR spectroscopy and were biologically investigated using phytobiological tests. Copyright