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(1-Benzenesulfonyl-cyclohexyl)-phosphonic acid diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130948-71-9

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130948-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130948-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,9,4 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130948-71:
(8*1)+(7*3)+(6*0)+(5*9)+(4*4)+(3*8)+(2*7)+(1*1)=129
129 % 10 = 9
So 130948-71-9 is a valid CAS Registry Number.

130948-71-9Relevant academic research and scientific papers

Facile solid-phase synthesis of cycloalkylphosphonates and 1-cycloalkenylphosphonates using polymer-supported phenylsulfonylmethylphosphonates

Liu, Xiao-Ling,Sheng, Shou-Ri,Zhou, Wei,Wang, Qin-Ying,Zhang, Xiao-Lan,Gong, Bin

, p. 119 - 127 (2007)

A facile procedure for the solid-phase synthesis of cycloalkylphosphonates and 1-cycloalkenylphosphonates in good yields and high purities using polystyrene-supported phenylsulfonylmethylphosphonates with traceless sulfone linker strategy is described. Copyright Taylor & Francis Group, LLC.

Convenient synthesis of cycloalkylphosphonates from (Phenylsulfonyl)methylphosphonate

Kim, Dae Young,Suh, Ki Hyung

, p. 83 - 91 (2007/10/03)

Cycloalkylphosphonate derivatives were synthesized in excellent overall yields, in two steps by the bis-alkylation of (phenyl sulfonyl)methylphosphonate with ω-dibromoalkanes in the presence of a phase transfer catalyst followed by desulfonation.

α-FUNCTIONAL CYCLOALKYLPHOSPHONATES. I. SYNTHESIS

Nasser, Jamal,About-Jaudet, Elie,Collignon, Noel

, p. 171 - 179 (2007/10/02)

Cycloalkylphosphonates 2 of different sizes (from cyclopropyl to cycloheptyl) bearing various functional groups Z in α-position were synthesized by bis-alkylation of α-functional methylphosphonates 1 and ω-dibromoalkanes in presence of base.The choice of the basic system is determined by the nature of Z.With powerful electron-withdrawing groups, NaH-THF/DMSO (Method A, for Z = CN, SO2R) or liquid-solid phase transfer process proved to be the more suitable systems.For Z = aryl or SR, lithium diisopropylamide is required to achieve the deprotonation.A wide range of new phoshonates were obtained in high yields on preparative scale.

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