6116-92-3

Basic information

• Product Name: 2(3H)-Oxazolone, 4,5-diphenyl-, hydrazone
• CAS NO: 6116-92-3
• Molecular Formula: C15H13N3O
• Molecular Weight: 251.288
• Mol File: 6116-92-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2(3H)-Oxazolone, 4,5-diphenyl-, hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Oxazolone, 4,5-diphenyl-, hydrazone(6116-92-3)
• EPA Substance Registry System: 2(3H)-Oxazolone, 4,5-diphenyl-, hydrazone(6116-92-3)

Safety Data

• Hazardous Substances Data: 6116-92-3(Hazardous Substances Data)

Usage

Chemical structure

Five-membered cyclic compound containing oxygen and nitrogen atoms, with phenyl groups at the 4 and 5 positions.

Classification

Hydrazone derivative of 2(3H)-Oxazolone.

Usage

Organic synthesis, ligands in metal complexes, and intermediates in the preparation of pharmaceutical compounds.

Distinct chemical properties

Presence of phenyl groups in the 4 and 5 positions of the oxazolone ring.

Need for further study

Specific properties and potential applications in various fields require further research and characterization.

Upstream product

• 5014-83-5 4,5-diphenyloxazol-2-one 
• 49656-04-4 2-Chlor-4,5-diphenyl-oxazol 

Downstream Products

• 139515-27-8 N-(4,5-Diphenyl-oxazol-2-yl)-N'-[1-pyridin-2-yl-meth-(E)-ylidene]-hydrazine 
• 85044-88-8 1-Benzyl-3-[(4,5-diphenyl-oxazol-2-yl)-hydrazono]-1,3-dihydro-indol-2-one 
• 6117-33-5 4-nitro-benzaldehyde (4,5-diphenyl-oxazol-2-yl)-hydrazone 
• 6117-44-8 (5,6-diphenyl-oxazolo[2,3-c][1,2,4]triazol-3-yl)-phenyl-amine 
• 6117-37-9 tribenzoyl-(4,5-diphenyl-oxazol-2-yl)-hydrazine 
• 139515-55-2 (2R,3S,4S)-5-((Z)-4-{1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-ethyl}-phenylimino)-pentane-1,2,3,4-tetraol 
• 85051-63-4 (2R,3R,4S)-5-((Z)-3-{1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-ethyl}-phenylimino)-pentane-1,2,3,4-tetraol 
• 85051-62-3 (2R,3S,4S)-5-((Z)-3-{1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-ethyl}-phenylimino)-pentane-1,2,3,4-tetraol 
• 139515-52-9 C₃₁H₂₆N₆O₂ 
• 139515-53-0 C₃₁H₂₆N₆O₂ 
• 139515-57-4 (2R,3R,4R,5R)-6-((Z)-3-{1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-ethyl}-phenylimino)-hexane-1,2,3,4,5-pentaol 
• 139515-54-1 ((E)-4-{1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-ethyl}-phenylimino)-acetic acid 
• 61930-45-8 ((E)-3-{1-[(4,5-Diphenyl-oxazol-2-yl)-hydrazono]-ethyl}-phenylimino)-acetic acid 
• 139515-44-9 N-(4,5-Diphenyl-oxazol-2-yl)-N'-[1-(4-fluoro-phenyl)-but-(E)-ylidene]-hydrazine 

Relevant articles and documents

3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: Inhibitors of immune complex induced inflammation

3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives were evaluated in the dermal and pleural reverse passive Arthus reactions in the rat. In the pleural test these compounds were effective in reducing exudate volume and accumulation of white blood cells. This pattern of activity was similar to that of hydrocortisone and different from that of indomethacin. The structural requirements for inhibiting the Arthus reactions were studied by systematic chemical modification of 1. These structure-activity relationship studies revealed that nitrogen 1' of the hydrazino group is essential for activity and must be electron rich, whereas chemical modifications of other sites of 1 had only a modest effect on activity.