113386-48-4

Basic information

• Product Name: 1-Phthalazinol, 2-(4-bromophenyl)-1,2-dihydro-
• CAS NO: 113386-48-4
• Molecular Formula: C14H11BrN2O
• Molecular Weight: 303.158
• Mol File: 113386-48-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Phthalazinol, 2-(4-bromophenyl)-1,2-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Phthalazinol, 2-(4-bromophenyl)-1,2-dihydro-(113386-48-4)
• EPA Substance Registry System: 1-Phthalazinol, 2-(4-bromophenyl)-1,2-dihydro-(113386-48-4)

Safety Data

• Hazardous Substances Data: 113386-48-4(Hazardous Substances Data)

Upstream product

• 643-79-8 o-phthalic dicarboxaldehyde 
• 622-88-8 4-bromophenylhydrazine hydrochloride 

Downstream Products

• 113386-54-2 (E)-2,2'-Bis-(4-bromo-phenyl)-2H,2'H-[1,1']biphthalazinylidene 
• 128174-79-8 2-(4-bromophenyl)-1(2H)-phthalazinone 
• 128278-57-9 2-(4-Bromo-phenyl)-1,2-dihydro-phthalazine 
• 128174-80-1 2-(4-Bromo-phenyl)-2H-phthalazine-1-thione 
• 128174-82-3 3-<2-(p-bromophenyl)-1,2-dihydrophthalazin-1-yl>-4-<2-(p-bromophenyl)-1,2-dihydrophthalazin-1-ylidene>-1-phenyl-3,4-dihydropyrrole-2,5-dione 

Relevant articles and documents

Simple Analogues of Quaternary Benzo[ c]phenanthridine Alkaloids: Discovery of a Novel Antifungal 2-Phenylphthalazin-2-ium Scaffold with Excellent Potency against Phytopathogenic Fungi

Inspired by sanguinarine and chelerythrine, a novel antifungal 2-phenylphthalazin-2-ium scaffold as a simple analogue was designed. Most of the 30 compounds showed excellent inhibition activity against almost all eight phytopathogenic fungi, far superior to sanguinarine and chelerythrine. A third of the compounds were more active than azoxystrobin in most cases. Compounds 26 and 27 showed the highest total activity against all the fungi with EC50 means of ca. 4.6 μg/mL. Fusarium solani showed the highest susceptibility with an EC50 mean of 3.62 μg/mL to 19 compounds. A concentration of 25.0 μg/mL 27 can fully control the Colletotrichum gloeosporioides infection in apples over 9 days. Electron microscopic observations showed that 27 was able to damage the structures of the hypha and cell membrane. The structure-activity relationship showed that the presence of electron-withdrawing groups on the C-ring increases the activity against most of the fungi. Thus, 2-phenylphthalazin-2-ium compounds represent promising leads for the development of novel fungicides.