4410-14-4

Basic information

• Product Name: 2-Phenylphenanthro[9,10-d]oxazole
• Synonyms: 2-Phenylphenanthro[9,10-d]oxazole
• CAS NO: 4410-14-4
• Molecular Formula: C₂₁H₁₃NO
• Molecular Weight: 295.33
• Mol File: 4410-14-4.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Phenylphenanthro[9,10-d]oxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenylphenanthro[9,10-d]oxazole(4410-14-4)
• EPA Substance Registry System: 2-Phenylphenanthro[9,10-d]oxazole(4410-14-4)

Safety Data

• Hazardous Substances Data: 4410-14-4(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 3942-85-6 10-imino-10H-phenanthren-9-one 
• 1077-18-5 N-benzylidenebutan-1-amine 
• 451-40-1 phenyl benzyl ketone 
• 100-52-7 benzaldehyde 
• 100-66-3 methoxybenzene 
• 84-11-7 9,10-phenanthrenequinone 
• 100-46-9 benzylamine 
• 89968-51-4 10-(methoxyimino)phenanthren-9-one 
• 140-11-4 Benzyl acetate 
• 100-39-0 benzyl bromide 
• 108-88-3 toluene 
• 618-31-5 benzylidene dibromide 
• 7664-41-7 ammonia 

Downstream Products

• 84-11-7 9,10-phenanthrenequinone 
• 65-85-0 benzoic acid 
• 85-01-8 phenanthrene 

Relevant articles and documents

The Voight reaction on tertiary α-hydroxy ketones

The Voight reaction is for the transformation of secondary α-hydroxy ketones into corresponding α-amino ketones. Although discovered as early as 1886, it has not enjoyed wide popularity in organic synthesis, as it is applicable to only secondary α-hydroxy

A novel compound, a method for preparing the same, and a negative active material for a redox flow battery including the new compound, and a redox flow battery comprising the same

The present invention provides a novel compound having an excellent redox stability and a low reduction potential. The present invention relates to a negative active material for a redox flow battery comprising a novel compound and a novel compound, and a

Synthesis of 5-(4-(1H-phenanthro[9,10-d]imidazol-2-yl)benzylidene)thiazolidine-2,4-dione as promising DNA and serum albumin-binding agents and evaluation of antitumor activity

A series of phenanthro[9,10-d]imidazole/oxazole and acenaphtho[1,2-d]imidazole with different aryl groups at C2-position has been synthesized. These compounds were in vitro evaluated for antitumor activity against a panel of 60 human cancer cell lines. Co

A convenient strategy to 2,4,5-triaryl and 2-alkyl-4,5-diaryl oxazole derivatives through silver-mediated oxidative CO cross coupling/cyclization

This is a silver(I) mediated Cα(sp3)H activation of primary amines followed by oxidative CO cross coupling/cyclization for the construction of 2,4,5-triaryl and 2-alkyl-4,5-diaryl oxazole derivatives. The protocol has been successfully utilized to synthesize the oxazole derivatives in good to excellent yields. In this oxidative coupling, the silver species after the reaction was successfully re-synthesized and reused with almost a similar activity.