42350-78-7

Usage

Uses

Due to the lack of specific applications provided in the materials, it is not possible to list the uses of (2-oxo-2-phenylethyl)(triphenyl)-lambda~5~-arsanyl. However, given its highly toxic nature, it is essential to handle and dispose of this chemical with proper caution and adherence to safety protocols to prevent severe health effects.

Upstream product

• 603-32-7 triphenyl-arsane 
• 70-11-1 α-bromoacetophenone 
• 22535-03-1 phenylacetyl bromide 
• 618-32-6 Benzoyl bromide 
• 20691-73-0 1-phenyl-2-triphenylarsoranyliden-ethanone 
• 108-86-1 bromobenzene 
• 24143-92-8 acetylmethylidene(triphenyl)-λ⁵-arsane 
• 106104-31-8 (2-benzoyloxystyryl)triphenylarsonium bromide 
• 127-09-3 sodium acetate 

Downstream Products

• 24721-26-4 4-chlorochalcone 
• 33555-17-8 2-phenyl-1H-benzo[g]indole 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 3558-24-5 1-methyl-2-phenyl-1H-indole 
• 6266-95-1 1-phenyl-2-<4-(N,N-dimethylamino)phenyl>ethanone 
• 54435-79-9 (E)-1,3-diphenyl-3-methyl-2-propen-1-one 
• 38829-78-6 2-phenyl-3H-benzo(e)indole 
• 22965-98-6 4-(dimethylamino)chalcone 
• 948-65-2 2-phenyl-indole 
• 82071-13-4 6-Methyl-3-phenyl-1,2-dihydro-cinnoline 
• 86001-88-9 triphenylarsineacetylbenzoylmethylene 
• 466686-18-0 (2E)-4-acetoxy-1,4-diphenylbut-2-en-1-one 
• 466686-20-4 (2E,4E)-6-acetoxy-1,6-diphenylhexa-2,4-dien-1-one 

Relevant academic research and scientific papers

Synthesis of olefins via a Wittig reaction mediated by triphenylarsine

An arsine-mediated Wittig reaction for the synthesis of olefins is described. After heating triphenylarsine in the presence of an activated alkyl bromide for 30?min, the resulting arsonium salt condensed with aldehydes in as little as 5?min at room temperature, yielding the olefins in high yields. Aromatic, heteroaromatic, and alkyl aldehydes were all suitable substrates for this process.

A general method for the rapid high yield preparation of pure arsonium salts. Preparation of (3-alkoxy-carbonyl-2-oxopropyl)triphenylarsonium bromides

An easy, rapid method for the preparation of arsonium salts of high yield and purity, by heating an alkyl halide and triphenylarsine as a melt at about 80 °C, is described.