5814-04-0

Basic information

• Product Name: 3-(2,4-dichlorobenzyl)-5-[(naphthalen-1-yloxy)methyl]-1,2,4-oxadiazole
• Synonyms: Cyclohexanecarboxylic acid, 2-(cyclohexylcarbonyl)hydrazide;N'-(cyclohexylcarbonyl)cyclohexanecarbohydrazide (non-preferred name)
• CAS NO: 5814-04-0
• Molecular Formula: C₁₄H₂₄N₂O₂
• Molecular Weight: 385.2434
• Mol File: 5814-04-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 578.1°C at 760 mmHg
• Flash Point: 303.4°C
• Density: 1.371g/cm³
• Vapor Pressure: 9.23E-13mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: 3-(2,4-dichlorobenzyl)-5-[(naphthalen-1-yloxy)methyl]-1,2,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2,4-dichlorobenzyl)-5-[(naphthalen-1-yloxy)methyl]-1,2,4-oxadiazole(5814-04-0)
• EPA Substance Registry System: 3-(2,4-dichlorobenzyl)-5-[(naphthalen-1-yloxy)methyl]-1,2,4-oxadiazole(5814-04-0)

Safety Data

• Hazardous Substances Data: 5814-04-0(Hazardous Substances Data)

Upstream product

• 6996-92-5 benzeneseleninic acid 
• 110-83-8 cyclohexene 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 36062-19-8 1,3-diaminoguanidine hydrochloride 
• 38941-47-8 cyclohexanecarbohydrazide 
• 3289-28-9 ethyl cyclohexanecarboxylate 

Downstream Products

• 86661-21-4 1,2-Bis(α-chlorcyclohexylmethylen)hydrazin 
• 16537-05-6 tert-butyl cyclohexanecarboxylate 
• 58884-48-3 3,6-Dicyclohexyl-1,2,4,5-tetrazin 
• 86661-08-7 3,6-Dicyclohexyl-1,4-dihydro-1,2,4,5-tetrazin 
• 86661-09-8 3,6-Dicyclohexyl-1-methyl-1,4-dihydro-1,2,4,5-tetrazin 
• 86661-13-4 3,6-Dicyclohexyl-1,2-dimethyl-1,2-dihydro-1,2,4,5-tetrazin 
• 86661-10-1 3,6-Dicyclohexyl-1,4-dimethyl-1,4-dihydro-1,2,4,5-tetrazin 
• 858785-70-3 N,N'-bis-cyclohexylmethyl-hydrazine 
• 23337-87-3 1-Cyclohexanoyl-2-cyclohexylmethylhydrazin 

Relevant articles and documents

Preparation of pivaloyl hydrazide in water: (Propanoic acid, 2,2-dimethyl-, hydrazide)

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Oxidation of Hydrazine Derivatives with Arylsulfonyl Peroxides

A new method for the generation of the azo function is reported.A series of hydrazine derivatives, which included alkyl- and arylhydrazines, monoacylhydrazides, and diacylhydrazides, was oxidized with m-(trifluoromethyl)benzenesulfonyl peroxide.Smooth conversion to the diimide was observed.The diimides then yielded products typical of normal degradation pathways.