1309930-27-5

Basic information

• Product Name: 2-[5-[4-(bromomethyl)phenyl]-1,3,4-oxadiazol-2-yl]-2-hydroxy-1(2H)-acenaphthylenone
• Synonyms: 2-[5-[4-(bromomethyl)phenyl]-1,3,4-oxadiazol-2-yl]-2-hydroxy-1(2H)-acenaphthylenone
• CAS NO: 1309930-27-5
• Molecular Weight: 421.25
• Mol File: 1309930-27-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-[5-[4-(bromomethyl)phenyl]-1,3,4-oxadiazol-2-yl]-2-hydroxy-1(2H)-acenaphthylenone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[5-[4-(bromomethyl)phenyl]-1,3,4-oxadiazol-2-yl]-2-hydroxy-1(2H)-acenaphthylenone(1309930-27-5)
• EPA Substance Registry System: 2-[5-[4-(bromomethyl)phenyl]-1,3,4-oxadiazol-2-yl]-2-hydroxy-1(2H)-acenaphthylenone(1309930-27-5)

Safety Data

• Hazardous Substances Data: 1309930-27-5(Hazardous Substances Data)

Upstream product

• 6232-88-8 4-bromomethylbenzoic Acid 
• 73789-56-7 N-isocyaniminotriphenylphosphorane 
• 82-86-0 acenaphthene quinone 

Relevant articles and documents

One-pot, three-component reaction of N-isocyanimino-triphenylphosphorane (Ph 3PNNC), acenaphthoquinone, and an aromatic carboxylic acid in water

Water was used as an efficient green solvent for the synthesis of sterically congested 1,3,4-oxadiazoles derivatives via a one-pot, three-component reaction of various aromatic carboxylic acids, acenaphthoquinone, and N-isocyanimino-triphenylphosphorane (

Synthesis of sterically congested 1,3,4-oxadiazole derivatives from aromatic carboxylic acids, acenaphthoquinone, and (N-isocyanimino) triphenylphosphorane

Reactions of (N-isocyanimino)triphenylphosphorane with acenaphthoquinone in the presence of aromatic carboxylic acids proceed smoothly at room temperature and under neutral conditions to afford sterically congested 1,3,4-oxadiazole derivatives in high yie