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(3S,11bS)-3-amino-9,11-bis(benzyloxy)-2,3,6,7-tetrahydro-1H-pyrido[2,1-a]isoquinolin-4(11bH)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

949463-53-0

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  • (3S,11bS)-3-amino-9,11-bis(benzyloxy)-2,3,6,7-tetrahydro-1H-pyrido[2,1-a]isoquinolin-4(11bH)-one

    Cas No: 949463-53-0

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949463-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 949463-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,4,6 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 949463-53:
(8*9)+(7*4)+(6*9)+(5*4)+(4*6)+(3*3)+(2*5)+(1*3)=220
220 % 10 = 0
So 949463-53-0 is a valid CAS Registry Number.

949463-53-0Relevant articles and documents

Formal synthesis of schulzeines B and C

Kuntiyong, Punlop,Akkarasamiyo, Sunisa,Piboonsrinakara, Nuanpan,Hemmara, Chitlada,Songthammawat, Poramate

, p. 8034 - 8040 (2011/11/06)

A formal synthesis of schulzeines B and C, marine natural products with inhibitory effect against α-glucosidase, has been achieved. The key reactions of the synthesis are N-acyliminium ion cyclization, Sharpless asymmetric dihydroxylation, olefin cross me

A new approach to the C28 fatty acid chain of the marine natural products schulzeines B and C: A concise diastereoselective total synthesis of(-)-schulzeine B

Yang, Chao,Bao, Yu-Hui,Liang, Pan,Ye, Jian-Liang,Wang, Ai-E.,Huang, Pei-Qiang

experimental part, p. 6281 - 6288 (2011/09/19)

An enantioselective approach to the C28 fatty acid chain of the marine natural products schulzeines B and C was established based on the l-tartaric acid derived C4 chiron 11 via successive 1,4-bis-chain elongation reactions and catal

Enantioselective synthesis of schulzeines B and C via a β-lactone-derived surrogate for bishomoserine aldehyde

Liu, Gang,Romo, Daniel

supporting information; experimental part, p. 1143 - 1146 (2009/07/25)

Enantioselective syntheses of the glucosidase inhibitors schulzeines B and C were achieved by employing a Pictet-Spengler reaction of a β-lactone-derived, masked bishomoserine aldehyde. Subsequent Corey-Link reaction unveiled an α-azido acid enabling cycl

Total syntheses of schulzeines B and C

Gurjar, Mukund K.,Pramanik, Chinmoy,Bhattasali, Debabrata,Ramana,Mohapatra, Debendra K.

, p. 6591 - 6594 (2008/02/10)

(Chemical Equation Presented) Schulzeines B (2) and C (3) were synthesized by a convergent strategy using epimeric tricyclic lactam building blocks, 4 and 5, and the C28 fatty acid side chain 6. Syntheses of tricyclic lactams (4/5) were achieved by Bischl

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