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(1R,2R,9aS)-1-(benzyloxy)-2-hydroxy-3(E)-isobutylidene-1-methyloctahydroquinolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153108-76-0

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153108-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153108-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,0 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 153108-76:
(8*1)+(7*5)+(6*3)+(5*1)+(4*0)+(3*8)+(2*7)+(1*6)=110
110 % 10 = 0
So 153108-76-0 is a valid CAS Registry Number.

153108-76-0Relevant academic research and scientific papers

Determination of absolute stereochemistry and an alternative synthesis of homopumiliotoxin 223G: Identification on chiral GC columns with the natural alkaloid

Kibayashi, Chihiro,Aoyagi, Sakae,Wang, Tzu-Chueh,Saito, Kosuke,Daly, John W.,Spande, Thomas F.

, p. 1157 - 1159 (2007/10/03)

An alternative asymmetric synthesis of (+)-(1S,9aS)-homopumiliotoxin 223G (1) was accomplished via (1R,2R,9aS)-1-(benzyloxy)-2-hydroxy-1-methyl-3[(E)-isobutylidene] quinolizidine (4), which was synthesized according to the intramolecular nickel(II)/chromium(II)-mediated cyclization of the N-(iodoalkenyl)aldehyde 2. Compound 4 was converted to the acetate and subjected to reduction with lithium in ammonia, whereupon deprotection of the O-benzyl group and removal of the acetoxyl group occurred in a single operation to afford (+)-homopumiliotoxin 223G. The same sequence using (±)-4 was applied to the synthesis of racemic 223G. Gas chromatography of a sample of racemic 223G showed no separation into enantiomers on four different cyclodextrin-based chiral GC columns. We found, however, that the O-acetates of (±)-223G gave a nearly baseline separation on either a β-cyclodextrin column or a permethylated β-cyclodextrin column. The O-acetate of synthetic (+)-223G was identical on either of these two columns, with the first eluting O-acetate from acetylated (±)-223G and also with the acetylated 223G present in a frog skin extract, thus allowing us to confirm unambiguously the 1S,9aS absolute configurations of natural 223G.

Highly stereoselective total syntheses of (+)-allopumiliotoxins 267A and 339A via intramolecular nickel(II)/chromium(II)-mediated cyclization

Aoyagi, Sakae,Wang, Tzu-Chueh,Kibayashi, Chihiro

, p. 11393 - 11409 (2007/10/02)

Remarkably high regio- and stereoselective approaches for the syntheses of dendrobatid alkaloids (+)allopumiliotoxin 267A and 339A have been develop. As a model study for these alkaloids, we initially undertook intramolecular chromium(II)-mediated cycliza

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