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Phosphonic acid, [(methylthio)phenylmethyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70660-15-0

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70660-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70660-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,6 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70660-15:
(7*7)+(6*0)+(5*6)+(4*6)+(3*0)+(2*1)+(1*5)=110
110 % 10 = 0
So 70660-15-0 is a valid CAS Registry Number.

70660-15-0Relevant academic research and scientific papers

REACTION OF PUMMERER REARRANGEMENT INTERMEDIATE WITH AROMATIC COMPOUNDS: A NOVEL SYNTHESIS OF 1-(SUBSTITUTED-ARYL)METHYLTHIOMETHANEPHOSPHONATES

Kim, Taek Hyeon,Kim, Dae Young,Oh, Dong Young

, p. 755 - 760 (2007/10/02)

Pummerer reaction intermediate(2) of methylsulfinylmethanephosphonate(1) has been found to react mildly with aromatic compounds in the presence of tin(IV) chloride to afford 1-(substituted-aryl)methylthiomethanephosphonates.

Carbon-Carbon Bond Forming Reactions via α-Phosphoryl-α-thio Carbocations

Ishibashi, Hiroyuki,Sato, Tatsunori,Irie, Maki,Ito, Masae,Ikeda, Masazumi

, p. 1095 - 1098 (2007/10/02)

Diethyl chloro(methylthio)methylphosphonate (3) reacted with arenes and alk-1-enes in the presence of a Lewis acid to give the Friedel-Crafts product (5) and the ene product (8), respectively.The Pummerer rearrangement product (4) derived from diethyl (methylsulphinyl)methylphosphonate (10) also reacted with alk-1-enes in trifluoroacetic acid to give the products (8).

ARYLATION OF α-PHOSPHORYL SULFIDES VIA THEIR PUMMERER REARRANGEMENT INTERMEDIATES GENERATED FROM THE CORRESPONDING SULFOXIDES

Stamos, Ioannis K.

, p. 6261 - 6262 (2007/10/02)

Various aryl groups were introduced directly into the α-position of α-phosphoryl sulfides by treating their sulfoxides with trifluoroacetic anhydride and then with tin(IV) chloride in the presence of excess of the aryl compound.

SYNTHESIS OF 1-(SUBSTITUTED-ARYL) METHYLTHIOMETHANEPHOSPHONATES BY FRIEDEL-CRAFTS REACTION OF AROMATIC COMPOUNDS WITH CHLORO(METHYLTHIO)METHANEPHOSPHONATE

Kim, Taek Hyeon,Oh, Dong Young

, p. 1165 - 1166 (2007/10/02)

Friedel-Crafts reaction of aromatic compounds with chloro(methylthio)methanephosphonate(1) under mild condition in the presence of Lewis acid affords 1-(substituted-aryl)methylthiomethanephosphonates(2).

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