3095-87-2

Basic information

• Product Name: bromodiphenylarsine
• Synonyms: bromodiphenylarsine
• CAS NO: 3095-87-2
• Molecular Weight: 309.037
• Mol File: 3095-87-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: bromodiphenylarsine(CAS DataBase Reference)
• NIST Chemistry Reference: bromodiphenylarsine(3095-87-2)
• EPA Substance Registry System: bromodiphenylarsine(3095-87-2)

Safety Data

• Hazardous Substances Data: 3095-87-2(Hazardous Substances Data)

Upstream product

• 603-32-7 triphenyl-arsane 
• 829-83-4 diphenylarsane 
• 598-21-0 2-Bromoacetyl bromide 
• 62824-81-1 dimethyl-phenyl-arsine oxide; hydrobromide 
• 3134-95-0 bis(diphenylarsenic) sulfide 
• 53332-60-8 ethyl-diphenyl-arsine oxide 
• 637-03-6 phenylarsine oxide 
• 712-48-1 chlorodiphenylarsine 
• 33756-33-1 triphenyl-arsine oxide; hydrobromide 
• 2215-16-9 bis(diphenylarsino)oxide 
• 10035-10-6 hydrogen bromide 
• 34837-55-3 Phenylselenyl bromide 
• 153921-22-3 Se-diphenylarsanyl 4-methylbenzenecarboselenoate 
• 60-29-7 diethyl ether 

Downstream Products

• 19980-77-9 1,4-bis-(diphenylarsino)-butane 
• 113106-97-1 (m-fluorophenyl)diphenylarsine 
• 38563-50-7 cyclohexyl-diphenyl-arsine 
• 21978-45-0 1.2-(As(C₆H₅)2)-1.2-C₂B₁₀H₁₀ 
• 41923-72-2 cyclohexyl-methyl-diphenyl-arsonium; iodide 
• 1499-33-8 triphenylmethylarsonium iodide 
• 857587-57-6 cyclohexyl-diphenyl-arsine oxide 
• 2887-09-4 diphenylmethylarsine oxide 
• 113106-96-0 (p-fluorophenyl)diphenylarsine 

Relevant articles and documents

Supramolecular architecture of [AsPh2Br2]2[(Br3)?…(Br2)…(Br3)?] obtained by bromination of (AsPh2)2S

Bromination of (AsPh2)2S leads to cleavage of the sulfide bridge to give AsPh2Br when 1 mol of bromine is used but with 2 mols the product is the polybromide, [AsPh2Br2]2[Br8], c

Synthesis and characterization of Se-organoarsanyl selenocarboxylates

Sodium selenocarboxylates were found to react with organoarsanyl chlorides Ph3-(n)AsCl(n) 1-3 (n = 1, 2, 3) to give the corresponding Se-organoarsanyl esters RCOSeAsPh2 (5), (RCOSe)2AsPh (6) and (RCOSe)3As (7) in good yields. The reaction of Se-diphenylarsanyl 4-methylbenzenecarboselenoate 5g with phenylselenenyl bromide and phenyltellurenyl iodide afforded the corresponding Se-phenyl-selenenyl 13 and Se-phenyltellurenyl esters 14 in moderate yields, while the reaction with sodium phenoxide gave sodium 4- methylbenzenecarboselenoate (4g), phenyl 4-methylbenzoate (11) and phenoxydiphenylarsine (12), indicating the attack of phenoxy anion to both the carbonyl carbon and arsenic atoms.