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Bromodiphenylarsine, also known as 2,2'-diphenyl-2-arsapropane, is an organoarsenic compound with the chemical formula C15H14AsBr. It is a colorless, crystalline solid that is soluble in organic solvents. Bromodiphenylarsine is primarily used as a chemical intermediate in the synthesis of various organoarsenic compounds, which have applications in the pharmaceutical, agrochemical, and materials science industries. Due to its potential toxicity and environmental impact, handling and disposal of bromodiphenylarsine must be done with proper safety precautions and in accordance with local regulations.

3095-87-2

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3095-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3095-87-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,9 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3095-87:
(6*3)+(5*0)+(4*9)+(3*5)+(2*8)+(1*7)=92
92 % 10 = 2
So 3095-87-2 is a valid CAS Registry Number.

3095-87-2Relevant academic research and scientific papers

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

Silaghi-Dumitrescu, Luminita,Attia, Amr A.A.,Silaghi-Dumitrescu, Radu,Blake, Alexander J.,Sowerby, D. Bryan

, p. 120 - 126 (2017/09/14)

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

Stable nickel catalysts for fast norbornene polymerization: Tuning reactivity

Casares, Juan A.,Espinet, Pablo,Martin-Alvarez, Jose M.,Martinez-Ilarduya, Jesus M.,Salas, Gorka

, p. 3825 - 3831 (2007/10/03)

The air-stable complexes trans-[Ni(C6Cl2F 3)2L2] (L = SbPh3, 1; AsPh 3, 2; AsCyPh2, 3; AsMePh2, 4; PPh3, 5) have been synthesized by arylation of

Synthesis and characterization of Se-organoarsanyl selenocarboxylates

Kanda,Mizoguchi,Koike,Murai,Kato

, p. 282 - 286 (2007/10/02)

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.

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