93418-12-3

Basic information

• Product Name: 4-chloro-N'-(thiophen-2-ylmethylidene)benzohydrazide
• Synonyms: 4-chloro-N'-(thiophen-2-ylmethylidene)benzohydrazide
• CAS NO: 93418-12-3
• Molecular Weight: 264.735
• Mol File: 93418-12-3.mol

Chemical Properties

• CAS DataBase Reference: 4-chloro-N'-(thiophen-2-ylmethylidene)benzohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-N'-(thiophen-2-ylmethylidene)benzohydrazide(93418-12-3)
• EPA Substance Registry System: 4-chloro-N'-(thiophen-2-ylmethylidene)benzohydrazide(93418-12-3)

Safety Data

• Hazardous Substances Data: 93418-12-3(Hazardous Substances Data)

Upstream product

• 98-03-3 thiophene-2-carbaldehyde 
• 536-40-3 4-chlorobenzoic acid hydrazide 

Downstream Products

• 102136-91-4 {TiCl₂(C₆H₄ClCONNCHC₄H₃S)2} 
• 119578-41-5 antimony(III)trichloride(TpClBHH) 
• 119578-42-6 antimony(III)Br₃(TpClBHH) 

Relevant articles and documents

Synthesis, antiproliferative activity and apoptosis-promoting effects of arene ruthenium(II) complexes with N, O chelating ligands

New half sandwich arene ruthenium(II) complexes of the type [Ru(arene)Cl(L)] (where arene = benzene and p-cymene, L = thiophene benzhydrazone ligands) have been synthesized from the reactions of the neutral precursor [Ru(arene) (μ-Cl) Cl]2 and

Synthesis, molecular structure and electrochemical properties of nickel(ii) benzhydrazone complexes: influence of ligand substitution on DNA/protein interaction, antioxidant activity and cytotoxicity

A series of new nickel(ii) benzhydrazone complexes having the general formula [Ni(L)2] (where L = thiophene aldehyde benzhydrazone) have been synthesized via the reaction of Ni(OAc)2·4H2O with 2 equivalents of benzhydrazon

Mechanistic differences between in vitro assays for hydrazone-based small molecule inhibitors of anthrax lethal factor

A systematically generated series of hydrazones were analyzed as potential inhibitors of anthrax lethal factor. The hydrazones were screened using one UV-based and two fluorescence-based in vitro assays. The study identified several inhibitors with IC50 values in the micromolar range, and importantly, significant differences in the types of inhibition were observed with the different assays.