23550-76-7

Usage

Uses

Used in Coordination Chemistry:
(1Z)-1-(1,3-benzodioxol-5-ylmethylidene)-2-phenylhydrazine is used as a ligand for the formation of coordination compounds. Its unique structure, including the benzodioxole ring and phenyl group, allows it to chelate with metal ions, potentially enhancing the stability and properties of the resulting complexes.
Used in Organic Synthesis:
As a precursor, (1Z)-1-(1,3-benzodioxol-5-ylmethylidene)-2-phenylhydrazine can be utilized in the synthesis of other organic molecules. Its hydrazine derivative nature and the presence of the benzodioxole ring may facilitate the creation of new compounds with specific functionalities and applications in various industries.
The specific properties and potential uses of (1Z)-1-(1,3-benzodioxol-5-ylmethylidene)-2-phenylhydrazine may be influenced by the methods of synthesis and purification, as well as the conditions under which it is employed. Further research and development would be necessary to fully explore and exploit its capabilities in different applications.

Upstream product

• 120-57-0 piperonal 
• 64-17-5 ethanol 
• 72358-76-0 phenylhydrazine acetate 
• 100-63-0 phenylhydrazine 
• 3510-50-7 anti-1,2-bis(benzo[d][1,3]dioxol-5-ylmethylene)hydrazine 
• 3510-50-7 {3,4-(OCH₂O)2C₆H₃C(H)=N-}2 
• 7732-18-5 water 
• 16742-62-4 3,4-methylenedioxybenzaldehyde semicarbazone 

Downstream Products

• 1622-13-5 3-benzo[1,3]dioxol-5-yl-1,5-diphenyl-formazan 
• 16742-62-4 3,4-methylenedioxybenzaldehyde semicarbazone 
• 64-17-5 ethanol 
• 64499-60-1 N-phenyl-piperonylamidine 
• 62031-32-7 phenylazo-piperonaldoxime 
• 35291-76-0 bis-benzo[1,3]dioxol-5-yl-ethanedione-bis-phenylhydrazone 
• 7684-30-2 N,N-dimethyl-N'-phenylcarbamimidic chloride 
• 4421-09-4 piperonylonitrile 
• 94255-59-1 (3,4-Methylendioxy-benzaldehyd)-(4-tricyanvinyl-phenylhydrazon) 
• 50656-08-1 N'-phenylbenzo[d][1,3]dioxole-5-carbohydrazonoyl chloride 
• 1416008-58-6 tert-butyl 5'-(benzo[d][1,3]dioxol-5-yl)-4'-tert-butyl-2-oxo-2'-phenyl-2',4'-dihydrospiro[indoline-3,3'-pyrazole]-1-carboxylate 
• 97935-96-1 3-Benzo[1,3]dioxol-5-yl-5-(4-chloro-phenyl)-1-phenyl-tetrahydro-pyrrolo[3,4-c]pyrazole-4,6-dione 
• 97935-90-5 3-Benzo[1,3]dioxol-5-yl-5-(4-methoxy-phenyl)-1-phenyl-1H-pyrrolo[3,4-c]pyrazole-4,6-dione 

Relevant academic research and scientific papers

sp2-C–H Acetoxylation of Diversely Substituted (E)-1-(Arylmethylene)-2-phenylhydrazines Using PhI(OAc)2 as Acetoxy Source at Ambient Conditions

A catalyst- and additive-free simple and straightforward method for regioselective direct sp2 C–H acetoxylation reaction of aldehyde hydrazones has been achieved at ambient temperature employing PIDA as an acetoxy source. The scope of the reaction has been successfully verified with a wide range of biologically important aldehyde hydrazones with diverse functional group tolerance. The method is highly selective, mild and efficient, operationally simple, rapid and high-yielding.

PYRAZOLE DERIVATIVES AS NHIBITORS OF THE WNT SIGNALLING PATHWAY

The present invention relates to a novel class of compounds as inhibitors of the Wnt signalling pathway. The best compounds showed potencies in the low micromolar range and high efficacies (> 80%) together with good microsomal stability. Furthermore, in v

Polystyrene sulfonic acid catalyzed greener synthesis of hydrazones in aqueous medium using microwaves

An environmentally benign aqueous protocol for the synthesis of cyclic, bi-cyclic, and heterocyclic hydrazones using polystyrene sulfonic acid (PSSA) as a catalyst has been developed; the simple reaction proceeds efficiently in water in the absence of any