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(3S,10bR)-3,5-diphenyl-3,10b-dihydro-2H-oxazolo[2,3-a]isoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1533409-58-3

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1533409-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1533409-58-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,3,4,0 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1533409-58:
(9*1)+(8*5)+(7*3)+(6*3)+(5*4)+(4*0)+(3*9)+(2*5)+(1*8)=153
153 % 10 = 3
So 1533409-58-3 is a valid CAS Registry Number.

1533409-58-3Downstream Products

1533409-58-3Relevant academic research and scientific papers

Au(III)-catalyzed regio-and stereoselective tandem synthesis of oxazolo fused naphthyridines and isoquinolines from o-alkynylaldehydes

Jha, Rajeev Ranjan,Danodia, Abhinandan Kumar,Kumar, Sushil,Verma, Akhilesh Kumar

supporting information, p. 610 - 615 (2014/01/23)

An efficient tandem approach for the regio-and stereoselective synthesis of oxazolo-fused naphthyridines 3a-g, 3i-l and isoquinolines 3h, 3m via the reaction of o-alkynylaldehydes 1a-i with chiral amino alcohols 2a-c under mild reaction conditions is described. The stereochemistry and structures of the products were assigned via NOESY and X-ray crystallographic studies.

Stereoselective tandem synthesis of oxazolo-fused pyrroloquinolines from o-alkynylaldehydes via Ag(I)-catalyzed regioselective 5-exo-dig ring closure

Jha, Rajeev Ranjan,Aggarwal, Trapti,Verma, Akhilesh Kumar

, p. 2603 - 2608 (2014/05/06)

A tandem approach for the regio- and stereoselective synthesis of oxazolo-fused pyrroloquinolines 3a-l via the reaction of o-alkynylaldehydes 1a-i with chiral amino alcohols 2a-c under mild reaction conditions is described. The possible participation of the pyridine ring in the regioselective formation of 5-exo-dig cyclized products was supported by the controlled experiments. The structures and stereochemistry of the products were confirmed by NOESY and X-ray crystallographic studies.

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