2588-85-4

Basic information

• Product Name: Benzenamine, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis-
• CAS NO: 2588-85-4
• Molecular Formula: C14H12N4O
• Molecular Weight: 252.275
• Mol File: 2588-85-4.mol

Chemical Properties

• CAS DataBase Reference: Benzenamine, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis-(2588-85-4)
• EPA Substance Registry System: Benzenamine, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis-(2588-85-4)

Safety Data

• Hazardous Substances Data: 2588-85-4(Hazardous Substances Data)

Upstream product

• 121-92-6 3-nitrobenzoic acid 
• 2491-89-6 2,5-bis-(3-nitro-phenyl)-[1,3,4]oxadiazole 

Downstream Products

• 725-12-2 2,5-bis-(phenyl)-1,3,4-oxadiazole 
• 1151394-14-7 C₃₂H₂₆N₆O₃ 

Relevant articles and documents

The Synthesis and Structure of a New Type of Aromatic Heterocyclic Macrocycle. IV. Synthesis of a 1,3,4-Oxadiazole-containing Azomacrocycle

A novel azomacrocycle containing the 1,3,4-oxadiazole ring has been prepared from 2,5-bis[3-(4-hydroxyphenylazo)phenyl]-1,3,4-oxadiazole 5 and 2,5-bis(2-chloromethlylphenyl)-1,3,4-oxadiazole 8. The coupling reaction between the diazonium salt 4 and bisphe

In silico design, synthesis, and screening of novel deoxyhypusine synthase inhibitors targeting HIV-1 replication

The human enzyme deoxyhypusine synthase (DHS) is an important host cell factor that participates in the post-translational hypusine modification of eukaryotic initiation factor 5A (eIF-5A). Hypusine-modified eIF-5A plays a role in a number of diseases, in

2,5-SUBSTITUTED OXAZOLE DERIVATIVES AS PROTEIN KINASE INHIBITORS FOR THE TREATMENT OF CANCER

Certain oxazole-based compounds exhibiting ATP-utilizing enzyme inhibitory activity, methods of using compounds exhibiting ATP-utilizing enzyme inhibitory activity, and compositions comprising compounds exhibiting ATP-utilizing enzyme inhibitory activity, are disclosed.

Structures of substituted di-aryl-1,3,4-oxadiazole derivatives: 2,5-bis(pyridyl)- and 2,5-bis(aminophenyl)-substitution

Crystal structures of four different di-aryl-1,3,4-oxadiazole compounds (aryl = 2-pyridyl-, 3-pyridyl-, 2-aminophenyl-, 3-aminophenyl-) are determined. Crystallization of di(2-pyridyl)-1,3,4-oxadiazole yielded monoclinic and triclinic polymorphs. The stru

Formation of exciplexes in films of polyimides, polyamides, and polyquinazolones derived from aromatic and heteroaromatic diamines

The emission bands exchibited by films of polyimides derived from 1,3-bis(3,4-dicarboxyphenoxy)benzene dianhydride, hexafluoroisopropylidenedibenzene-3,3′,4,4′-tetracarboxylic dianhydride, and aromatic and heteroaromatic diamines, and also of polyamides and polyquinazolones derived from the same amines are exciplex bahnds. With polyamides, complexes in the ground state are formed. The fluorescence of the photoconductivity sensitizer Rhodamine 6G is quenched in films of these polymers by the exciplex mechanism. 2005 Pleiades Publishing, Inc.