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558346

Sigma-Aldrich

4-Methoxybenzhydrazide

97%

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About This Item

Linear Formula:
H3COC6H4CONHNH2
CAS Number:
Molecular Weight:
166.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

solid

mp

136-140 °C (lit.)

functional group

amine
hydrazine

SMILES string

COc1ccc(cc1)C(=O)NN

InChI

1S/C8H10N2O2/c1-12-7-4-2-6(3-5-7)8(11)10-9/h2-5H,9H2,1H3,(H,10,11)

InChI key

REKQLYUAUXYJSZ-UHFFFAOYSA-N

Application

4-Methoxybenzhydrazide may be used to synthesize:
  • N′-[(E)-5-bromo-2-hydroxy-3-methoxybenzylidene]-4-methoxybenzohydrazide monohydrate
  • 2,5-bis(4-methoxyphenyl)-1,3,4-oxadiazole
  • hydrazone ligands, which readily forms ruthenium(II) hydrazone complexes via reaction with [RuHCl(CO)(PPh3)3]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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2, 5-Bis (4-methoxyphenyl)-1, 3, 4-oxadiazole.
Fun HK, et al.
Acta Crystallographica Section B, Structural Science, Crystal Engineering and Materials, 66(12), o3072-o3072 (2010)
N'-[(E)-5-Bromo-2-hydroxy-3-methoxybenzylidene]-4-methoxybenzohydrazide monohydrate.
Reshma PR, et al.
Acta Crystallographica Section B, Structural Science, Crystal Engineering and Materials, 68(10), o2821-o2822 (2012)
Ruthenium (II) complexes containing 4-methoxybenzhydrazone ligands: synthesis, characterization, DNA binding, DNA cleavage, radical scavenging and in vitro cytotoxic activity.
Mohanraj M, et al.
Applied Organometallic Chemistry, 30(7), 550-560 (2016)
Cheuk-Fai Chow et al.
Chemistry, an Asian journal, 3(8-9), 1324-1335 (2008-07-30)
Nine neutral dynamic metallosupramolecular polymers (metallodynamers) based on acyl hydrazone derived metal coordination centers (Co(2+), Ni(2+), Zn(2+), and Cd(2+)) were generated through self-assembly polymerization. These are linear coordination polymers with specific optical and mechanical properties. Monomer selection was found to

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