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(2-Bromo-2-phenylethyl)diphenylphosphine oxide is a complex organic compound with the chemical formula C19H16BrOP. It is a derivative of diphenylphosphine oxide, featuring a 2-bromo-2-phenylethyl group attached to the phosphorus atom. (2-bromo-2-phenylethyl)diphenylphosphine oxide is characterized by its unique structure, which includes a phosphorus atom bonded to two phenyl rings and an oxygen atom, with a bromine atom and a phenylethyl group attached to the carbon atom adjacent to the phosphorus. It is a colorless solid and is used in various chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals, due to its ability to act as a ligand or a reagent. The compound's properties, such as its reactivity and stability, make it a valuable intermediate in organic synthesis.

3582-85-2

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3582-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3582-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3582-85:
(6*3)+(5*5)+(4*8)+(3*2)+(2*8)+(1*5)=102
102 % 10 = 2
So 3582-85-2 is a valid CAS Registry Number.

3582-85-2Downstream Products

3582-85-2Relevant academic research and scientific papers

Copper-catalyzed hydrophosphinations of styrenes in water at room temperature

Isley, Nicholas A.,Linstadt, Roscoe T. H.,Slack, Eric D.,Lipshutz, Bruce H.

, p. 13196 - 13200 (2014)

Copper-catalyzed hydrophosphinations of styrenyl systems in water, at room temperature is herein reported, enabled by our 'designer' surfactant TPGS-750-M. This is an attractive alternative to the more common Pd and Pt catalyzed versions.

Phosphinoyl Radical Initiated Vicinal Cyanophosphinoylation of Alkenes

Zhang, Pei-Zhi,Zhang, Ling,Li, Jian-An,Shoberu, Adedamola,Zou, Jian-Ping,Zhang, Wei

supporting information, p. 5537 - 5540 (2017/10/25)

A double-functionalization reaction of alkenes through Mn(OAc)3-mediated phosphinoyl radical addition followed by CuCN-catalyzed cyanation is introduced. This one-pot reaction is performed under mild conditions to afford vicinal cyanophosphinoylation products.

Direct radical acetoxyphosphorylation of styrenes mediated by manganese(III)

Zhou, Shao-Fang,Li, Da-Peng,Liu, Kui,Zou, Jian-Ping,Asekun, Olayinka Taiwo

, p. 1214 - 1220 (2015/01/30)

Direct radical acetoxyphosphorylation of styrenes mediated by Mn(OAc)3 with diphenylphosphine oxide and dialkyl phosphites was described, and a new type of difunctionalization of alkenes was achieved.

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