24090-92-4

Basic information

• Product Name: N'-(naphthalen-1-ylmethylene)benzohydrazide
• Synonyms: N'-(naphthalen-1-ylmethylene)benzohydrazide
• CAS NO: 24090-92-4
• Molecular Weight: 274.322
• Mol File: 24090-92-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N'-(naphthalen-1-ylmethylene)benzohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N'-(naphthalen-1-ylmethylene)benzohydrazide(24090-92-4)
• EPA Substance Registry System: N'-(naphthalen-1-ylmethylene)benzohydrazide(24090-92-4)

Safety Data

• Hazardous Substances Data: 24090-92-4(Hazardous Substances Data)

Upstream product

• 93-58-3 benzoic acid methyl ester 
• 65-85-0 benzoic acid 
• 66-77-3 1-naphthaldehyde 
• 613-94-5 benzoic acid hydrazide 

Downstream Products

• 1191940-86-9 C₂₂H₂₁ClN₂O₃ 
• 1236309-98-0 C₂₂H₁₈N₂O₂ 
• 1259388-10-7 N'-(2,2-difluoro-1-(naphthalen-1-yl)-3-oxo-3-phenylpropyl)benzohydrazide 
• 1366284-33-4 N-(2,2-difluoro-1-(naphthalen-1-yl)-3-oxo-3-phenylpropyl)benzohydrazide 
• 1429926-31-7 C₁₈H₁₃ClN₂OPd 
• 1429926-33-9 C₃₆H₂₇N₂OPPd 
• 1610886-46-8 C₅₄H₄₃IrN₂OP₂ 
• 1476076-90-0 trans-[Ru(nabhH)(PPh₃)2Cl] 
• 897-18-7 2-(1-naphthyl)-5-phenyl-1,3,4-oxadiazole 
• 1010796-51-6 C₂₁H₂₀N₂O 

Relevant articles and documents

Analogs of Nitrofuran Antibiotics to Combat Resistance

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Iron(III)/TEMPO-Catalyzed Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazoles by Oxidative Cyclization under Mild Conditions

A simple and efficient cationic Fe(III)/TEMPO-catalyzed oxidative cyclization of aroyl hydrazones has been developed for the synthesis of 2,5-disubstituted 1,3,4-oxadiazole derivatives. The reaction offers a broad scope, good functional-group tolerance, and high yields under mild conditions in the presence of O 2.

Efficient oxidative cyclization of N -acylhydrazones for the synthesis of 2,5-disubstituted 1,3,4-oxadiazoles using t-BuOI under neutral conditions

An efficient procedure for the oxidative cyclization of N -acylhydrazones was developed utilizing tert-butyl hypoiodite (t-BuOI), which is generated in situ from t -BuOCl and NaI. A variety of 2,5-disubstituted 1,3,4-oxadiazoles were synthesized in high yields within short reaction time. The method is also suitable for cyclization of N -acylhydrazones derived from heterocyclic aldehydes and aliphatic aldehydes. Mild reaction conditions and simple workup operations make the procedure a good alternative for the synthesis of 2,5-disubstituted 1,3,4-oxadiazoles.