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10409-56-0

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10409-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10409-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,0 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10409-56:
(7*1)+(6*0)+(5*4)+(4*0)+(3*9)+(2*5)+(1*6)=70
70 % 10 = 0
So 10409-56-0 is a valid CAS Registry Number.

10409-56-0Relevant articles and documents

Reaction of silyl enol ethers with phosphite using hypervalent iodine compound: A new synthesis of 2-aryl-2-oxoalkylphosphonates

Dae Young Kim,Joo Yang Mang,Dong Young Oh

, p. 629 - 634 (1994)

Reaction of phosphite with silyl enol ethers using iodosobenzene/boron trifluoride etherate provides a direct route for the preparation of 2-aryl- 2-oxoalkylphosphonates in good yields.

Copper-Catalyzed Microwave-Expedited Oxyphosphorylation of Alkynes with Diethyl Phosphite and t-Butyl Hydroperoxide Synthesis of Densely Functionalized Phosphonylated Indenones

Maciás-Benítez, Pablo,Sierra-Padilla, Alfonso,Tenorio, Manuel J.,Moreno-Dorado, F. Javier,Guerra, Francisco M.

, p. 16409 - 16424 (2021/11/16)

Treatment of alkynes with diethyl phosphite and t-butyl hydroperoxide in the presence of [Cu(MeCN)4]BF4 under microwave irradiation produced the oxyphosphorylation of the triple bond, giving rise to the corresponding β-ketophosphonates in moderate-to-good yields. When the triple bond was conjugated to a carbonyl group bearing an aromatic ring, it led to the cyclization of the resulting ketone intermediate, producing eventually different phosphonylated indenones.

Preparation method for synthesizing beta-carbonyl phosphonate derivatives via olefin

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Paragraph 0055; 0056; 0057, (2017/08/25)

The invention discloses a method for synthesizing beta-carbonyl phosphonate derivatives via olefin and belongs to the field of organic chemistry. In the method, olefin (or olefin acid) and H-phosphite are used as raw materials, CuSO4.5H2O is used as a catalyst, and beta-carbonyl phosphonate derivatives are synthesized by heating reaction. The method is cheap and readily available in raw materials, simple in operation, mild in reaction condition and high in synthetic yield, and is suitable for industrialized production. The derivatives are often used as intermediates for synthesizing alpha, beta-unsaturated carbonyl compounds, and the derivatives also have wide bioactivity and significant metal compounding capability and play an irreplaceable role in medicinal chemistry, biological chemistry and inorganic chemistry.

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