54608-83-2

Basic information

• Product Name: 3,5-bis(p-nitrophenyl)-1,2,4-oxadiazole
• Synonyms: 3,5-bis(p-nitrophenyl)-1,2,4-oxadiazole
• CAS NO: 54608-83-2
• Molecular Weight: 312.241
• Mol File: 54608-83-2.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 3,5-bis(p-nitrophenyl)-1,2,4-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-bis(p-nitrophenyl)-1,2,4-oxadiazole(54608-83-2)
• EPA Substance Registry System: 3,5-bis(p-nitrophenyl)-1,2,4-oxadiazole(54608-83-2)

Safety Data

• Hazardous Substances Data: 54608-83-2(Hazardous Substances Data)

Upstream product

• 192332-48-2 (Z)-4-nitrobenzamidoxime 
• 68451-95-6 (Z)-4-nitro-N'-((4-nitrobenzoyl)oxy)benzimidamide 
• 1613-86-1 N-hydroxy-4-nitrobenzamidine 
• 122-04-3 4-nitro-benzoyl chloride 
• 2574-03-0 p-nitrobenzonitrile oxide 
• 61713-82-4 3,5-bis(p-nitrophenyl)-1,2,4-oxadiazole 4-oxide 
• 1011-84-3 4-nitrobenzohydroximoyl chloride 
• 188118-39-0 N,N-Diethyl-N'-hydroxy-4-nitro-benzamidine 
• 58402-81-6 (Z)-4-nitrobenzohydroximoyl chloride 
• 619-72-7 4-nitrobenzonitrile 
• 108-30-5 succinic acid anhydride 
• 192332-48-2 N'-hydroxy-4-nitrobenzimidamide 
• 109-92-2 ethyl vinyl ether 
• 4231-71-4 1H-1,2,3-benzotriazol-1-yl-4-nitrophenylmethanone 

Relevant articles and documents

The reaction of amidoximes with carboxylic acids or their esters under high-pressure conditions

3,5-Disubstituted 1,2,4-oxadiazoles were synthesized by the reaction of amidoximes with carboxylic acids or their esters under high-pressure conditions (10 kbar). The reaction proceeds without the use of other reagents or catalysts. Both aliphatic and aro

Synthesis and Properties of Energetic 1,2,4-Oxadiazoles

The synthesis and characterization of a series of 3,5-di-aryl-1,2,4-oxadiazoles are reported and the effects of nitro groups in the aromatic rings on the experimental heats of decomposition (ΔHd) and heats of combustion (ΔHc) are evaluated. Heats of formation (ΔHf) and densities (ρ) were calculated and correlations between ΔHd and ΔHf were assessed for these compounds. Experimental determination of ρ (by gas pycnometry) on a selection of the compounds led to the calculation of detonation velocity (VD), detonation pressure (PD) and specific impulse (ISP) parameters by the Explo 5 program. An X-ray analysis of compound (4i) confirmed the structure and showed a crystal density (at 120 K) close to that determined by gas pycnometry.

Improved microwave-mediated synthesis of 3-(3-aryl-1,2,4-oxadiazol-5-yl) propionic acids and their larvicidal and fungal growth inhibitory properties

The synthesis of 3-(3-aryl-1,2,4-oxadiazol-5-yl)propionic acids from arylamidoximes and succinic anhydride under focused microwave irradiation conditions is described. The new synthetic method furnished the desired products in 2-3 min and good yields. Fur