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138604-24-7

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138604-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138604-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,0 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138604-24:
(8*1)+(7*3)+(6*8)+(5*6)+(4*0)+(3*4)+(2*2)+(1*4)=127
127 % 10 = 7
So 138604-24-7 is a valid CAS Registry Number.

138604-24-7Relevant articles and documents

Palladium catalyzed asymmetric reactions assisted by P*,P*-bidentate bisdiamidophosphites based on 1,4-diols

Gavrilov, Konstantin N.,Zheglov, Sergey V.,Gavrilov, Vladislav K.,Maksimova, Marina G.,Tafeenko, Viktor A.,Chernyshev, Vladimir V.,Birin, Kirill P.,Mikhel, Igor S.

, p. 461 - 471 (2017/01/13)

A small series of P*,P*-bidentate bisdiamidophosphite ligands containing 1,3,2-diazaphospholidine rings have been prepared. The cationic [Pd(allyl)(P*,P*)]BF4and neutral [Pd(P*,P*)Cl2] palladium(II) complexes were synthesized with on

Nonsimple relationships between the P*-chiral diamidophosphite and the arylphosphine moieties in Pd-catalyzed asymmetric reactions: Combinatorial approach and P,P*-bidentate phosphine-diamidophosphites

Gavrilov, Konstantin N.,Shiryaev, Alexei A.,Zheglov, Sergey V.,Gavrilov, Vladislav K.,Groshkin, Nikolay N.,Maksimova, Marina G.,Volov, Alexandr N.,Zamilatskov, Ilya A.

, p. 616 - 624 (2014/02/14)

A small family of P,P*-bidentate C1-symmetric ligands containing 1,3,2-diazaphospholidine rings with stereogenic phosphorus atoms has been prepared. Palladium catalytic systems with these phosphine-diamidophosphites afforded 95% and

Application of pyranoside phosphite-pyridine ligands to enantioselective metal-catalyzed allylic substitutions and conjugate 1,4-additions

Lega, Matteo,Margalef, Jessica,Ruffo, Francesco,Pamies, Oscar,Dieguez, Montserrat

, p. 995 - 1000 (2013/09/23)

A series of glucopyranoside phosphite-pyridine ligands have been applied in the metal-catalyzed allylic substitution and conjugate 1,4-addition reactions of several substrate types. We have been able to identify ligands that provided promising enantioselectivities in the Pd-catalyzed intermolecular allylic substitution of cyclic substrates (ee's up to 86%) and desymmetrization (ee's up to 94%) and in the Cu-catalyzed conjugate addition of challenging aliphatic enones (ee's up to 90%).

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