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tert-butyl 2,3-dihydro-1-oxo-3-phenyl-1H-indene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1041024-78-5

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1041024-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041024-78-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,0,2 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1041024-78:
(9*1)+(8*0)+(7*4)+(6*1)+(5*0)+(4*2)+(3*4)+(2*7)+(1*8)=85
85 % 10 = 5
So 1041024-78-5 is a valid CAS Registry Number.

1041024-78-5Relevant academic research and scientific papers

Enantio- and diastereoselective catalytic alkylation reactions with aziridines

Moss, Thomas A.,Fenwick, David R.,Dixon, Darren J.

, p. 10076 - 10077 (2008)

The first asymmetric phase transfer catalyzed alkylation reaction of a range of carbon acids with N-sulfonyl aziridines is reported. When 10 mol % of a cinchona derived quaternary ammonium salt was employed as the catalyst under mildly basic conditions, N

Organocatalytic Michael addition of indanone carboxylates to vinyl selenone for the asymmetric synthesis of polycyclic pyrrolidines

Sternativo, Silvia,Walczak, Ola,Battistelli, Benedetta,Testaferri, Lorenzo,Marini, Francesca

, p. 10536 - 10541,6 (2012/12/12)

A Michael addition of racemic indanone carboxylates to vinyl selenone catalyzed by C6′hydroxyl cinchona derivatives is the key step of a synthetic sequence for a practical access to highly enantioenriched (up to 98% ee) polycyclic pyrrolidines bearing contiguous tertiary and quaternary stereocenters.

Organocatalytic Michael addition of indanone carboxylates to vinyl selenone for the asymmetric synthesis of polycyclic pyrrolidines

Sternativo, Silvia,Walczak, Ola,Battistelli, Benedetta,Testaferri, Lorenzo,Marini, Francesca

, p. 10536 - 10541 (2013/01/15)

A Michael addition of racemic indanone carboxylates to vinyl selenone catalyzed by C6′hydroxyl cinchona derivatives is the key step of a synthetic sequence for a practical access to highly enantioenriched (up to 98% ee) polycyclic pyrrolidines bearing contiguous tertiary and quaternary stereocenters.

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