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Boronic acid, [2-(1-cyclohexen-1-yl)ethenyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138375-81-2

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138375-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138375-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138375-81:
(8*1)+(7*3)+(6*8)+(5*3)+(4*7)+(3*5)+(2*8)+(1*1)=152
152 % 10 = 2
So 138375-81-2 is a valid CAS Registry Number.

138375-81-2Downstream Products

138375-81-2Relevant academic research and scientific papers

Fast synthesis of complex enantiopure heterocyclic scaffolds by a tandem sequence of simple transformations on α-hydroxyaldehydes

Cannillo, Alexandre,Norsikian, Stephanie,Retailleau, Pascal,Dau, Marie-Elise Tran Huu,Iorga, Bogdan I.,Beau, Jean-Marie

, p. 9127 - 9131 (2013)

Two tandems are faster than one! Properly sequenced reactions initiated by the Petasis aminoalcohol synthesis from boronic acids, diallylamine, and α-hydroxyaldehydes, including free aldoses, leads to rapid construction of complex enantiopure structures (see scheme). Copyright

Palladium catalysed tandem cyclisation-anion capture. Part 8: Cascade hydrostannylation-cyclisation-anion capture and cascade hydroboration-cyclisation-anion capture on solid phase

Grigg, Ronald,MacLachlan, William S,MacPherson, David T,Sridharan, Visuvanathar,Suganthan, Selvaratnam

, p. 10335 - 10345 (2007/10/03)

Up to four bonds and five stereocentres are created, in five component processes (five point diversity), utilising resin bound aryl iodides by hydroboration or hydrostannylation of alkynes, followed by cyclisation-anion capture involving Suzuki or Stille reactions. Three small libraries were prepared to validate the chemistry.

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