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137742-81-5

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137742-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137742-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,4 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 137742-81:
(8*1)+(7*3)+(6*7)+(5*7)+(4*4)+(3*2)+(2*8)+(1*1)=145
145 % 10 = 5
So 137742-81-5 is a valid CAS Registry Number.

137742-81-5Downstream Products

137742-81-5Relevant articles and documents

Rearrangement of phenylethenes on reaction with iodine-xenon difluoride

Patrick, Timothy B.,Qian, Suntian

, p. 3359 - 3360 (2000)

(matrix presented) Phenyl-substituted ethenes react with iodine and xenon difluoride to provide difluorinated products. Iodofluoro intermediates react with xenon difluoride to produce transient iodine difluoride species that lose IF and F- and produce carbocations.

N-Fluorobisimides: Reactions with Some Olefins via α-Fluoro Carbocationic Intermediates

DesMarteau, Darryl D.,Xu, Ze-Qi,Witz, Michael

, p. 629 - 635 (2007/10/02)

N-Fluorobisimides are a new class of electrophilic fluorinating agents.Reaction of (CF3SO2)2NF (1) with olefins gave various products, depending on the reaction conditions and the structure of the substrate.In solvents of higher nucleophilicity such as H2O, acetic acid, aqueous HCl, and (HF)nPy, α-fluorohydrins and their acetates, α,β-chlorofluoro- and α,β-difluoroalkanes were obtained.In acetic acid, trans-stilbene and tetraphenylethylene produced the rearranged, nonfluorinated aldehyde and ketone.Evidence is presented for the reactions proceeding via a one-electron transfer mechanism involving α-fluorocarbocationic intermediates.

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