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(2R,6R)-6-Isopropoxy-2-((E)-styryl)-3,6-dihydro-2H-pyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

336181-56-7

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336181-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 336181-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,1,8 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 336181-56:
(8*3)+(7*3)+(6*6)+(5*1)+(4*8)+(3*1)+(2*5)+(1*6)=137
137 % 10 = 7
So 336181-56-7 is a valid CAS Registry Number.

336181-56-7Relevant academic research and scientific papers

Synthesis of unsaturated lactone moieties by asymmetric hetero Diels-Alder reactions with binaphthol-titanium complexes

Quitschalle, Monika,Christmann, Mathias,Bhatt, Ulhas,Kalesse, Markus

, p. 1263 - 1265 (2001)

Natural products like ratjadone and callystatin A contain an α,β-unsaturated lactone moiety which adds to the biological activity of these compounds. Here we report a rapid and practical access to lactone precursor 3 by an asymmetric hetero Diels-Alder reaction as the key step and its subsequent transformation into a suitable building block 4.

The cytotoxic styryl lactone goniothalamin is an inhibitor of nucleocytoplasmic transport

Wach, Jean-Yves,Güttinger, Stephan,Kutay, Ulrike,Gademann, Karl

supporting information; experimental part, p. 2843 - 2846 (2010/07/16)

An in vivo nuclear export assay (immunostaining of Rio2 in HeLa cells) demonstrated that (R)-goniothalamin is an inhibitor of nucleocytoplasmic transport above 500 nM, which was rationalized also by molecular modeling. The cytotoxic styryl lactone natural product was prepared via an enantioselective Cr(III) catalyzed hetero Diels-Alder reaction and a Sonogashira coupling. A series of analogs was synthesized and only the oxidized goniothalamin derivative featuring an alkyne spacer was found active. Unsaturated lactones of natural origin other than leptomycin (LMB) are thus suggested to operate via a similar mechanism targeting the CRM1 nuclear receptor.

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