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140870-79-7

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140870-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140870-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,7 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140870-79:
(8*1)+(7*4)+(6*0)+(5*8)+(4*7)+(3*0)+(2*7)+(1*9)=127
127 % 10 = 7
So 140870-79-7 is a valid CAS Registry Number.

140870-79-7Downstream Products

140870-79-7Relevant academic research and scientific papers

Scandium-catalyzed carbon-carbon bond formations using α- organosulfanyl and organoselanyl-α-fluoroacetic acid derivatives

Gotoh, Kohei,Yamamoto, Teruhisa,Yoshimatsu, Mitsuhiro

, p. 1611 - 1615 (2007/10/03)

The scandium-catalyzed reactions of α-organosulfanyl and organoselanyl-α-fluoroacetates 1-2, acetamides 3-4 and acetonitrile 5 with soft nucleophiles proceeded to give the products 6a-b, 7a-c, 8a-c, 9a-e in good to high yields. We also successfully perfor

Fluorinations of α-seleno carboxylic acid derivatives with hypervalent (difluoroiodo)toluene

Arrica, Maria A.,Wirth, Thomas

, p. 395 - 403 (2007/10/03)

A very efficient synthesis of (difluoroiodo)toluene avoiding the use of elemental chlorine and elemental fluorine is described. We have fluorinated a series of α-acceptor substituted selenides using (difluoroiodo)toluene. The reactions are usually very clean and under the reaction conditions no further oxidized products are observed. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.

ELECTROLYTIC PARTIAL FLUORINATION OF ORGANIC COMPOUNDS. 3. REGIOSELECTIVE ANODIC MONOFLUORINATION OF ORGANOSELENIUM COMPOUNDS AND THEIR SYNTHETIC APPLICATION

Fuchigami, Toshio,Hayashi, Toshiaki,Konno, Akinori

, p. 3161 - 3164 (2007/10/02)

Regioselective anodic α-monofluorination of selenides bearing electron-withdrawing groups such as cyano, ester, and amide groups was successfully performed.Highly stereoselective synthesis of α-fluoro α,β-unsaturated esters was achieved by using an α-fluo

Fluoride ion promoted anodic substitutions of chalcogeno compounds.2. Regioselective anodic methoxylation of 1,1-dihydro-perfluoroalkyl and cyanomethyl selenides

Surowiec,Fuchigami

, p. 1065 - 1068 (2007/10/02)

Anodic methoxylation of 1,1-dihydroperfluoroalkyl and cyanomethyl selenides was achieved in the presence of Et3N·3HF as a supporting electrolyte.

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