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(2R,6R,8S)-9-(benzyloxy)-2-[(4S,5S)-2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl]-6,8-dimethylnon-4-yn-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1257329-16-0

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1257329-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1257329-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,3,2 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1257329-16:
(9*1)+(8*2)+(7*5)+(6*7)+(5*3)+(4*2)+(3*9)+(2*1)+(1*6)=160
160 % 10 = 0
So 1257329-16-0 is a valid CAS Registry Number.

1257329-16-0Downstream Products

1257329-16-0Relevant articles and documents

A highly stereoselective total synthesis of (+)-9-epi-dictyostatin

Zanato, Chiara,Pignataro, Luca,Ambrosi, Andrea,Hao, Zhongyan,Gennari, Cesare

, p. 5767 - 5771 (2010)

The total synthesis of (+)-9-epi-dictyostatin (1b), a diastereomer of the antimitotic marine-sponge-derived macrolide (-)-dictyostatin (1a), was achieved by creating 11 stereogenic centers and 4 stereogenic double bonds with a high level of stereocontrol.

Highly stereoselective total synthesis of (+)-9-epi-Dictyostatin and (-)-12,13-Bis-epi-dictyostatin

Zanato, Chiara,Pignataro, Luca,Ambrosi, Andrea,Hao, Zhongyan,Trigili, Chiara,Diaz, Jose Fernando,Barasoain, Isabel,Gennari, Cesare

, p. 2643 - 2661 (2011/06/25)

The total syntheses of (+)-9-epi-dictyostatin (1a) and (-)-12,13-bis-epi- dictyostatin (1b), diastereomers of the antimitotic marine sponge-derived macrolide (-)-dictyostatin (1), were achieved by creating 11 stereogenic centers and 4stereogenic double bonds with a high level of stereocontrol. The yield for the 29-step longest linear sequence from Roche ester was 1.53 and 1.52%, respectively. The final key steps to these unnatural products were the addition of vinylzincates C10-C26 to aldehyde C1-C9 (leading surprisingly to complete stereoselectivity for the 9R-configuration in 28a and for the 9S-configuration in 12,13-bis-epimeric 28b), followed by Yamaguchi macrolactonization and global deprotection. (-)-12,13-Bis-epi-dictyostatin (1b) displayed a dramatic decrease of cytotoxicity and of the affinity toward the paclitaxel binding site of microtubules. Eleven stereogenic centers and fourstereogenic double bonds were obtained with a high level of stereocontrol in the total synthesis of (+)-9-epi-dictyostatin and(-)-12,13-bis-epi-dictyostatin, diastereomers of the antimitotic marine sponge-derived macrolide (-)-dictyostatin.

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