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Se-phenyl diphenylselenophosphinate is a chemical compound with the molecular formula C18H15PSe. It is a derivative of phosphorus and selenium, featuring a phenyl group (C6H5) attached to a phosphorus atom, which in turn is bonded to a selenium atom. The selenium atom is also connected to another phenyl group, making the compound a diphenylselenophosphinate. This organophosphorus compound is known for its potential applications in various fields, including as a ligand in coordination chemistry, a reagent in organic synthesis, and a precursor in the preparation of other organophosphorus compounds. Its unique structure and properties make it a subject of interest in chemical research and development.

2049-62-9

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2049-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2049-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2049-62:
(6*2)+(5*0)+(4*4)+(3*9)+(2*6)+(1*2)=69
69 % 10 = 9
So 2049-62-9 is a valid CAS Registry Number.

2049-62-9Downstream Products

2049-62-9Relevant academic research and scientific papers

Electrochemical selenation of phosphonates and phosphine oxides

Guo, Shengmei,Li, Sen,Zhang, Zhebin,Yan, Wenjie,Cai, Hu

, (2020)

An environmentally friendly electrocatalytic strategy for the synthesis of organoselenophospho-rus between phosphonates /phosphine oxides and selenols/diselenides is reported. The reaction was performed with metal-, base- and oxidant-free at room temperat

Accelerating Electrochemical Synthesis through Automated Flow: Efficient Synthesis of Chalcogenophosphites

Amri, Nasser,Wirth, Thomas

supporting information, p. 1894 - 1898 (2020/11/24)

Integrated electrochemical reactors in automated flow systems have been utilised for chalcogenophosphite formations. Multiple electrochemical reactions can be performed using a programmed sequence in a fully autonomous way. Differently functionalised chal

Photoinduced Coupling Reaction of Diphenyl(2,4,6-trimethylbenzoyl)phosphine Oxide with Interelement Compounds: Application to the Synthesis of Thio- or Selenophosphinates

Sato, Yuki,Kawaguchi, Shin-Ichi,Nomoto, Akihiro,Ogawa, Akiya

, p. 3558 - 3567 (2017/08/16)

Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TMDPO) is a radical initiator widely used in the field of macromolecular chemistry, but not often applied in synthetic organic chemistry. We have focused on the use of TMDPO as a phosphorus source in reactions with different E - E compounds, where E - E represents a heteroatom-heteroatom bond, under photoirradiation. Interestingly, the cross-coupling reaction between TMDPO and disulfides or diselenides successfully affords thio- or selenophosphinates and thio- or selenoesters, respectively. The synthesis of series of thio- and selenophosphinates by this photoinduced cross-coupling reaction is demonstrated.

Chloroform-based Atherton-Todd-type reactions of alcohols and thiols with secondary phosphine oxides generating phosphinothioates and phosphinates

Li, Shan,Chen, Tieqiao,Saga, Yuta,Han, Li-Biao

, p. 71544 - 71546 (2015/09/08)

Chloroform-based Atherton-Todd-type reactions of alcohols and thiols with secondary phosphine oxides, generating phosphinothioates and phosphinates, respectively, are described. Various valuable phosphinothioates and phosphinates including those with functional groups are readily prepared under mild reaction conditions.

Rhodium-catalyzed highly stereoselective hydroselenation of internal alkynes bearing an electron-withdrawing group

Kawaguchi, Shin-Ichi,Kotani, Mao,Atobe, Shingo,Nomoto, Akihiro,Sonoda, Motohiro,Ogawa, Akiya

experimental part, p. 6766 - 6769 (2012/02/05)

Rhodium-catalyzed highly regio- and stereoselective hydroselenation of internal alkynes bearing an electron-withdrawing group took place to give (E)-vinyl selenides in good yields. The excellent syn stereoselectivity of this rhodium-catalyzed hydroselenation is of great importance in terms of complementing the previously reported hydroselenation of alkynes.

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