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methyl (1S,3R,3aS,6aR)-5-ethyl-4,6-dioxo-3-phenyloctahydro pyrrolo[3,4-c]pyrrole-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1140972-17-3

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1140972-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1140972-17-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,0,9,7 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1140972-17:
(9*1)+(8*1)+(7*4)+(6*0)+(5*9)+(4*7)+(3*2)+(2*1)+(1*7)=133
133 % 10 = 3
So 1140972-17-3 is a valid CAS Registry Number.

1140972-17-3Downstream Products

1140972-17-3Relevant academic research and scientific papers

Binap-silver salts as chiral catalysts for the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and alkenes

Mancebo-Aracil, Juan,Martin-Rodriguez, Maria,Najera, Carmen,Sansano, Jose M.,Costa, Paulo R.R.,De Lima, Evanoel Crizanto,Dias, Ayres G.

, p. 1596 - 1606 (2013/02/23)

Binap-AgSbF6 catalyzed 1,3-dipolar cycloadditions between azomethine ylides and electrophilic alkenes are described and compared with analogous transformations mediated by other Binap-silver(I) salt complexes. Maleimides and 1,2-bis(phenylsulfo

Binap-gold(I) versus Binap-silver trifluoroacetate complexes as catalysts in 1,3-dipolar cycloadditions of azomethine ylides

Martin-Rodriguez, Maria,Najera, Carmen,Sansano, Jose M.,De Cozar, Abel,Cossio, Fernando P.

experimental part, p. 14224 - 14233 (2012/01/06)

The 1,3-dipolar cycloaddition between azomethine ylides and alkenes is efficiently catalysed by [{(Sa)-Binap-Au(tfa)}2] (Binap=2,2′-bis(diphenylphosphino)-1,1′-binaphthyl; tfa=trifluoroacetyl). Maleimides, 1,2-bis(phenylsulfonyl)ethy

Binap-gold(I) trifluoroacetate as a bifunctional catalyst for the synthesis of chiral prolines through 1,3-dipolar cycloaddition of azomethine ylides

Martin-Rodriguez, Maria,Najera, Carmen,Sansano, Jose M.,Wu, Feng-Liu

experimental part, p. 1184 - 1186 (2010/11/02)

Highly enantioselective 1,3-dipolar cycloadditions of amino acid-derived azomethine ylides with alkenes have been performed, for the first time, under gold-catalysis using (Sa)-or (Ra)-Binap-gold(I) trifluoroacetate complexes, with t

BINAP-AgSbF6 vs. BINAP-AgClO4 complexes as catalysts for the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and alkenes

Martín-Rodríguez, María,Nájera, Carmen,Sansano, José M.,Costa, Paulo R. R.,De Lima, Evanoel Crizanto,Dias, Ayres G.

experimental part, p. 962 - 966 (2010/07/10)

The employment of AgSbF6 and BINAP ligands has been evaluated in the catalyzed enantioselective 1,3-dipolar cycloadditions between azomethine ylides and electrophilic alkenes. The results are compared with the analogous ones obtained when using

Synthesis of prolines by enantioselective 1,3-dipolar cycloaddition of azomethine ylides and alkenes catalyzed by chiral phosphoramidite-silver(I) complexes

Najera, Carmen,De Retamosa, Maria Gracia,Martin-Rodriguez, Maria,Sansano, Jose M.,De Cozar, Abel,Cossio, Fernando P.

experimental part, p. 5622 - 5634 (2010/03/01)

The endo-diastereo- and enantioselective 1,3-dipolar cyclo-addition of azomethine ylides and electrophilic alkenes is ef-ficiently catalysed by chiral phosphoramidite-silver(I) Per-chlorate complexes. The reaction allows the presence of dif-ferent types o

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