75128-85-7

Upstream product

• 75150-37-7 anthrione 
• 74001-89-1 (3-Chloro-benzylidene)-triphenyl-λ⁵-arsane 
• 77032-87-2 Anthracen-9-yl-(3-chloro-phenyl)-methanol 
• 77032-91-8 9-[Chloro-(3-chloro-phenyl)-methyl]-anthracene 

Downstream Products

• 77033-24-0 9-(3-Chloro-benzyl)-anthracene 

Relevant academic research and scientific papers

Reactions of (9-Anthryl)arylmethyl Chloride and Its Homologues with Nucleophiles under Solvolytic Conditions. Notable Effects of Reaction Conditions and Substituents on the Reaction Sites

The reactions of (9-anthryl)arylmethyl chlorides 2a-e (the substituents are p-MeO, p-Me, H, p-Cl, and m-Cl), the corresponding bromides 3b-d (the substituents are p-Me, H, and p-Cl), and the antimonate salts 4b-e (the substituents are p-Me, H, p-Cl, and m

Studies on Betaine Decomposition of Arsonium Ylides

A systematic study on the nature of decomposition of betaine formed by nucleophilic attack of semistabilized arsonium ylides on thiocarbonyl substrates has been carried out.A series of substituted benzylidenetriphenylarsenanes have been generated from their corresponding salts and condensed with few cyclic thioketones to yield exocyclic olefins as exclusive products.The non-availability of thioepoxides indicates that the mode of decomposition of such type of betaines is quite analogous to the betaine formed by phosphonium ylides.The structure of the products have been assigned by IR and NMR spectral studies. - Keywords: Betaine, Arsonium Ylides