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dimethyl (3-methylphenyl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15286-12-1

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15286-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15286-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15286-12:
(7*1)+(6*5)+(5*2)+(4*8)+(3*6)+(2*1)+(1*2)=101
101 % 10 = 1
So 15286-12-1 is a valid CAS Registry Number.

15286-12-1Downstream Products

15286-12-1Relevant academic research and scientific papers

A palladium-catalyzed oxidative cross-coupling reaction between aryl pinacol boronates and H-phosphonates in ethanol

Chen, Te-Hsuan,Reddy, Daggula Mallikarjuna,Lee, Chin-Fa

, p. 30214 - 30220 (2017)

The first successful oxidative coupling reaction of aryl pinacol boronic esters with H-phosphonates to deliver aryl phosphorous compounds is reported herein. These reactions between aryl boronic reagents and H-phosphonates were carried out synergistically using a Pd catalyst, additive and oxidant. Without using bases and ligands, phosphorylation was accomplished in an environmentally-friendly manner under mild conditions in ethanol.

C-P bond formation of cyclophanyl-, and aryl halides: Via a UV-induced photo Arbuzov reaction: A versatile portal to phosphonate-grafted scaffolds

Br?se, Stefan,Hassan, Zahid,Nieger, Martin,O?wald, Simon,Zippel, Christoph

, p. 3309 - 3312 (2022/02/11)

A new versatile method for the C-P bond formation of (hetero)aryl halides with trimethyl phosphite via a UV-induced photo-Arbuzov reaction, accessing diverse phosphonate-grafted arenes, heteroarenes and co-facially stacked cyclophanes under mild reaction

Photoinduced Transition-Metal-Free Cross-Coupling of Aryl Halides with H-Phosphonates

Zeng, Huiying,Dou, Qian,Li, Chao-Jun

supporting information, p. 1301 - 1305 (2019/02/19)

Photoinduced transition-metal- and photosensitizer-free cross-coupling of aryl halides (including Ar-Cl, Ar-Br, and Ar-I) with H-phosphonates (including dialkyl phosphonates and diarylphosphine oxides) is reported. Various functional groups were tolerated, including ester, methoxy, dimethoxy, alkyl, phenyl, trifluoromethyl, and heterocyclic compounds. This simple and green strategy provides a practical pathway to synthesize arylphosphine oxides.

A mild electroassisted synthesis of (hetero)arylphosphonates

Sengmany, Stéphane,Ollivier, Anthony,Le Gall, Erwan,Léonel, Eric

supporting information, p. 4495 - 4500 (2018/06/29)

The electrochemically-assisted synthesis of (hetero)arylphosphonates from (hetero)aryl halides and dimethyl phosphite is described. Very mild and simple conditions are employed as the cross-coupling is carried out in galvanostatic mode, in an undivided ce

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