78053-66-4

Basic information

• Product Name: 1-(phenylethynyl)anthra-9,10-quinone
• Synonyms: 1-(phenylethynyl)anthra-9,10-quinone
• CAS NO: 78053-66-4
• Molecular Formula: C₂₂H₁₂O₂
• Molecular Weight: 308.32948
• Mol File: 78053-66-4.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(phenylethynyl)anthra-9,10-quinone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(phenylethynyl)anthra-9,10-quinone(78053-66-4)
• EPA Substance Registry System: 1-(phenylethynyl)anthra-9,10-quinone(78053-66-4)

Safety Data

• Hazardous Substances Data: 78053-66-4(Hazardous Substances Data)

Upstream product

• 72307-77-8 1-Ethynylanthracene 
• 120-12-7 anthracene 
• 7396-21-6 1-acetylanthracene 
• 3485-80-1 1-iodo-9,10-anthraquinone 
• 536-74-3 phenylacetylene 
• 82-44-0 1-chloroanthracene-9,10-dione 
• 13146-23-1 copper(I) phenylacetylenide 

Downstream Products

• 1175017-82-9 C₂₂H₁₃NO₂ 
• 1175017-81-8 2-amino-3-benzoyl-7H-dibenzo[de,h]quinolin-7-one 
• 936-49-2 2-phenyl-2-imidazoline 
• 954-07-4 1-methylanthraquinone 
• 155269-07-1 4H-3-phenylanthra<9,1-c,d>-1,2-diazepin-8-one 
• 83790-96-9 1-(1,2-dioxo-2-phenylethyl)anthraquinone 

Relevant articles and documents

An unexpected rearrangement that disassembles alkyne moiety through formal nitrogen atom insertion between two acetylenic carbons and related cascade transformations: New approach to Sampangine derivatives and polycyclic aromatic amides

(Chemical Equation Presented) This work analyzes multiple new reaction pathways which originate from intramolecular reactions of activated alkynes with the appropriately positioned multifunctional hemiaminal moiety. Combination of experimental substituent

ACETYLENIC CONDENSATION AS A METHOD FOR THE SYNTHESIS OF ETHYNYLANTHRAQUINONES

The substitution of the iodine atom in 1- and 2-iodoanthraquinones and 1-iodo-4-nitroanthraquinone by a phenylethynyl residue was realized under various conditions.In the reaction of 1-iodoanthraquinone with phenylacetylene the formation of an anomalous p