63452-43-7

Usage

Type of compound

Hydrazine derivative

Substituents

Phenyl group, benzylidene group

Attachment to nitrogen atom

Both phenyl and benzylidene groups

Methoxy groups

Three (CH3O-) groups

Positions of methoxy groups

3, 4, and 5 on the benzene ring

Potential applications

Medicinal and pharmaceutical research

Contributing functional groups

Hydrazine and benzylidene

Biological activity

Possible due to functional groups and chemical structure

Pharmacological properties

Potentially influenced by hydrazine and benzylidene groups

Importance for research

Chemical structure and reactivity make it a potentially interesting compound for drug development and studying biologically active molecules.

Upstream product

• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 100-63-0 phenylhydrazine 
• 62-53-3 aniline 
• 59-88-1 phenylhydrazine hydrochloride 

Downstream Products

• 7684-30-2 N,N-dimethyl-N'-phenylcarbamimidic chloride 
• 1885-35-4 3,4,5-trimethoxybenzonitrile 
• 97935-89-2 5-(4-Methoxy-phenyl)-1-phenyl-3-(3,4,5-trimethoxy-phenyl)-3a,6a-dihydro-1H-pyrrolo[3,4-c]pyrazole-4,6-dione 
• 97935-93-8 5-(4-Methoxy-phenyl)-1-phenyl-3-(3,4,5-trimethoxy-phenyl)-1H-pyrrolo[3,4-c]pyrazole-4,6-dione 
• 97936-05-5 1,5-Diphenyl-3-(3,4,5-trimethoxy-phenyl)-tetrahydro-pyrrolo[3,4-c]pyrazole-4,6-dione 
• 1376268-47-1 3,5-bis(3,4,5-trimethoxyphenyl)-1-phenyl-1H-1,2,4-triazole 
• 90255-77-9 2-(3,4,5-trimethoxybenzylidene)-1-benzyl-1-phenylhydrazine 

Relevant academic research and scientific papers

Highly efficient donor-acceptor hydrazone dyes-inorganic Si/TiO2 hybrid solar cells

We have synthesized the two donor-bridge-acceptor organic dyes (hydrazone dye 1 (HD1) and hydrazone dye 2 (HD2)) with the aim to enhance intra-molecular charge transfer then characterized by FTIR and NMR. The ground state geometries have been optimized at

Stereospecific copper(II)-catalyzed tandem ring opening/oxidative alkylation of donor-acceptor cyclopropanes with hydrazones: Synthesis of tetrahydropyridazines

Aerobic copper(II)-catalyzed tandem ring opening and oxidative C-H alkylation of donor-acceptor cyclopropanes with bisaryl hydrazones is accomplished to produce tetrahydropyridazines, in which copper(II) plays dual role as a Lewis acid as well as redox catalyst. The reaction is stereospecific, and optically active cyclopropanes can be reacted with high optical purities (89-98% enantiomeric excess). The substrate scope, functional group tolerance, dual role of the copper(II) catalyst, and the use of air as an oxidant are the important practical features. A product bearing a 3-bromoaryl group can be subjected to Pd-catalyzed Suzuki coupling with boronic acid in high yield.

Copper-mediated synthesis of substituted 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles via C-H functionalization/C-N/C-O bond formation

An efficient method for the transformation of N-benzyl bisarylhydrazones and bisaryloxime ethers to functionalized 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles is described. The protocol involves a copper(II)-mediated cascade C-H functionalization/C-N/C-O bond formation under neutral conditions. Substrates having either electron-donating or -withdrawing substituents undergo the cyclization to afford the target heterocycles at moderate temperature.

Magnesium perchlorate as an efficient catalyst for the synthesis of imines and phenylhydrazones

Magnesium perchlorate has been found to be an efficient catalyst for the synthesis of imines and phenylhydrazones by the reaction of carbonyl compounds with amines and phenylhydrazine in high yields at room temperatures and in short times. The condensation of less electrophilic carbonyl compounds with poorly nucleophilic amines affords the imines in excellent yields.