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ethyl trimethylsilyl phenylphosphonite is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126709-30-6

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126709-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126709-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,0 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 126709-30:
(8*1)+(7*2)+(6*6)+(5*7)+(4*0)+(3*9)+(2*3)+(1*0)=126
126 % 10 = 6
So 126709-30-6 is a valid CAS Registry Number.

126709-30-6Relevant academic research and scientific papers

New synthesis of trimethylsilyl esters of phosphorus(III) acids

Morgalyuk, Vasily,Strelkova, Tatyana,Brel, Valery

, p. 1993 - 1997 (2019)

Abstract: A novel synthetically important reaction has been developed for the quick, convenient, and high-yield preparation of trimethylsilyl esters of phosphorus(III) acids, synthetically valuable Michaelis–Arbuzov reaction precursors. Commercially and synthetically available initial compounds used are derivatives of propan-2-ol phosphorylated in the second position capable of long-term storage and available silylating reagents: hexamethyldisilazane, bis(trimethylsilyl)acetamide, and diethyl(trimethylsilyl)amine. Also, a stepwise reaction scheme of the starting compounds with silylating reagents has been proposed. Graphic abstract: [Figure not available: see fulltext.].

An efficient synthesis of cis-4-hydroxyphosphonic and cis-4-hydroxyphosphinic analogs of pipecolic acid from cyclic enaminones

Argüello-Velasco, Rubén Oswaldo,Morales-Solís, Juan Carlos,Mu?oz-Vidales, Misael,Ordó?ez, Mario,Romero-Estudillo, Ivan,Viveros-Ceballos, José Luis

, (2022/01/24)

An expedient synthetic entry to cis-4-hydroxyphosphonic and cis-4-hydroxyphosphinic analogs of cis-4-hydroxypipecolic acid is presented in this paper. The main feature of this methodology is the highly regioselective addition of silyl phosphites or phosph

Chlorosilane-Catalyzed Coupling of Hydrogen Phosphine Oxides with Acyl Chlorides Generating Acylphosphine Oxides

Zhang, Jian-Qiu,Han, Li-Biao

supporting information, p. 4633 - 4637 (2020/06/23)

We report a new method for the synthesis of acylphosphine oxides by the direct coupling of hydrogen phosphine oxides and acyl chlorides mediated by chlorosilanes. This new protocol is greener and safer, because it precludes the generation of volatile haloalkanes and the use of oxidants employed in the conventional methods. Moreover, moisture-unstable acylphosphine oxides that are difficult to prepare via the conventional methods can be generated using this new method.

SYNTHESIS AND STEREOCHEMISTRY OF α-ARYL-β-NITROALKYLPHOSPHINATES

Li, Yu-Gui,Liu, Yun-Shan,Miao, Fang-Ming,Liu, Xiao-Lan,Cao, Jin-Hong,et al.

, p. 229 - 242 (2007/10/02)

An one-pot reaction of O-alkyl arylphosphonites 1 with α-aryl-β-nitroalkenes (β-nitrostyrenes) 2 in the presence of trimethylsilylchloride and triethylamine was studied.Twenty-three new α-aryl-β-nitroalkylphosphinates 3a-y were synthesized in high yield u

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