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Benzene, 1-[(R)-[(1Z)-2-iodoethenyl]sulfinyl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145070-59-3

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145070-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145070-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,7 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145070-59:
(8*1)+(7*4)+(6*5)+(5*0)+(4*7)+(3*0)+(2*5)+(1*9)=113
113 % 10 = 3
So 145070-59-3 is a valid CAS Registry Number.

145070-59-3Relevant academic research and scientific papers

Synthesis and diastereoselective complexation of enantiopure sulfinyl dienes: The preparation of sulfinyl iron(0) dienes

Paley, Robert S.,De Dios, Alfonso,Estroff, Lara A.,Lafontaine, Jennifer A.,Montero, Carlos,McCulley, David J.,Rubio, M. Belen,Ventura, Maria Paz,Weers, Heather L.,De la Pradilla, Roberto Fernandez,Castro, Sonia,Dorado, Rocio,Morente, Miguel

, p. 6326 - 6343 (2007/10/03)

The preparation of a diverse array of enantiomerically pure 1- and 2- sulfinyl dienes has been achieved via Stille coupling of halovinyl sulfoxides and vinyl stannanes, hydrogenation of 1-sulfinyl-1-en-3-ynes, or vinylcupration of 1-sulfinyl alkynes. Form

Synthesis of Enantiopure 2-Malonylvinyl Sulfoxides via Addition-Elimination Reactions of 2-Halo- and 2-(Mesyloxy)vinyl Sulfoxides

Marino, Joseph P.,Laborde, Edgardo,Deering, Carl F.,Paley, Robert S.,Ventura, Maria Paz

, p. 3193 - 3201 (2007/10/02)

Enantiomerically pure (E)-2-bromo- and (E)-2-iodovinyl sulfoxides 3a and 3b have been prepared in multigram quantities from (E)-1,2-bis(tri-n-butylstannyl)ethene; enantiomerically pure (E)-2-(mesyloxy)vinyl sulfoxide 3c has been synthesized by reaction of

Synthesis of enantiomerically pure (Z)-2-haloalkenyl sulfoxides

De La Pradilla, Roberto Fernandez,Morente, Miguel,Paley, Robert S.

, p. 6101 - 6102 (2007/10/02)

Efficient procedures to prepare enantiomerically pure (Z)-2-haloalkenyl sulfoxides from alkynyl sulfoxides are described.

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