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tert-butyl(((3S,4S)-5-((4-methoxybenzyl)oxy)-4-methylpent-1-yn-3-yl)oxy)dimethylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1393364-40-3

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1393364-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393364-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,3,6 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1393364-40:
(9*1)+(8*3)+(7*9)+(6*3)+(5*3)+(4*6)+(3*4)+(2*4)+(1*0)=173
173 % 10 = 3
So 1393364-40-3 is a valid CAS Registry Number.

1393364-40-3Relevant academic research and scientific papers

Modular synthesis of polyene side chain analogues of the potent macrolide antibiotic etnangien by a flexible coupling strategy based on hetero-bis-metallated alkenes

Altendorfer, Mario,Raja, Aruna,Sasse, Florenz,Irschik, Herbert,Menche, Dirk

, p. 2116 - 2139 (2013/04/23)

An efficient procedure for the concise synthesis of hetero-bis-metallated alkenes as useful building blocks for the modular access to highly elaborate polyenes and stabilized analogues is reported. By applying these bifunctional olefins in convergent Stille/Suzuki-Miyaura couplings, novel, carefully selected side chain analogues of the potent RNA polymerase inhibitor etnangien were synthesized by a modular late stage coupling strategy and evaluated for antibacterial and antiproliferative activities. The Royal Society of Chemistry 2013.

Efficient synthesis of diverse hetero-bis-metallated alkenes as modular reagents towards highly conjugated and isolated olefinic systems

Altendorfer, Mario,Menche, Dirk

, p. 8267 - 8269 (2012/09/21)

An efficient synthesis of diverse hetero-bis-metallated alkenes with conjugated and isolated olefin subunits is reported. Relying on those useful tin/boron reagents a convergent, palladium-catalyzed fragment coupling strategy has been developed as an eleg

Design, synthesis and biological evaluation of simplified side chains of the macrolide antibiotic etnangien

Altendorfer, Mario,Irschik, Herbert,Menche, Dirk

, p. 5731 - 5734 (2012/10/07)

Novel simplified side chains of the potent RNA polymerase inhibitor etnangien were designed, synthesized and evaluated for antibacterial activity against Gram-positive bacteria and one Gram-negative bacterium.

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