54918-94-4

Basic information

• Product Name: 1-[(2,4-dichlorophenoxy)acetyl]-2-(2-hydroxybenzylidene)hydrazine
• Synonyms: 1-[(2,4-dichlorophenoxy)acetyl]-2-(2-hydroxybenzylidene)hydrazine
• CAS NO: 54918-94-4
• Molecular Weight: 339.178
• Mol File: 54918-94-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-[(2,4-dichlorophenoxy)acetyl]-2-(2-hydroxybenzylidene)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(2,4-dichlorophenoxy)acetyl]-2-(2-hydroxybenzylidene)hydrazine(54918-94-4)
• EPA Substance Registry System: 1-[(2,4-dichlorophenoxy)acetyl]-2-(2-hydroxybenzylidene)hydrazine(54918-94-4)

Safety Data

• Hazardous Substances Data: 54918-94-4(Hazardous Substances Data)

Upstream product

• 90-02-8 salicylaldehyde 
• 28236-62-6 2,4-dichlorophenoxyacetylhydrazine 
• 89-95-2 2-methyl-benzyl alcohol 
• 94-75-7 2,4-Dichlorophenoxyacetic acid 
• 533-23-3 ethyl 2,4-dichlorophenoxyacetate 
• 774-74-3 2-(2,4-dichlorophenoxy)acetyl chloride 
• 1928-38-7 methyl 2,4-dichlorophenoxyacetate 

Downstream Products

• 160257-50-1 Cu₂(Cl₂C₆H₃OCH₂C(O)NHNCHC₆H₄O)2(ONO₂)⁽¹⁺⁾*NO₃^(1-)=[Cu₂(Cl₂C₆H₃OCH₂C(O)NHNCHC₆H₄O)2(ONO₂)]NO₃ 
• 160257-51-2 Cu₂(Cl₂C₆H₃OCH₂C(O)NNCHC₆H₄O)2(C₂H₅OH)(H₂O)=[Cu₂(Cl₂C₆H₃OCH₂C(O)NNCHC₆H₄O)2(C₂H₅OH)(H₂O)] 
• 160257-52-3 Cu₂(Cl₂C₆H₃OCH₂C(O)NNCHC₆H₄O)2(H₂O)2=[Cu₂(Cl₂C₆H₃OCH₂C(O)NNCHC₆H₄O)2(H₂O)2] 
• 160985-57-9 Ni(H₂O)2(OH)(OC₆H₄CHNNHC(O)CH₂OC₆H₃Cl₂) 
• 160985-57-9 Ni(OC₆H₄CHNNC(O)CH₂OC₆H₃Cl₂)(H₂O)3 

Relevant articles and documents

Facile solid state ball milling as a green strategy to prepare 2-(2,4-dichlorophenoxy)-N′-(2-hydroxybenzylidene)acetohydrazide complexes

2-(2,4-Dichlorophenoxy)-N′-(2-hydroxybenzylidene)acetohydrazide (H2L) complexes were prepared by ball milling involving the reaction of ligand with Ni(II), Co(II), Cu(II) and VO(II) salts (mechanochemical syntheses). The compounds were elucidat

An expedient method for the synthesis of acylhydrazones under microwave irradiation in solvent-free medium

A simple, efficient and eco-friendly method for the synthesis of acylhydrazones from acylhydrazides and aldehydes under microwave (MW) irradiation was reported, no solvent and catalyst was used. The method is combined with a combinatorial approach and fou