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6-(tert-Butyl-dimethyl-silanyloxy)-6-[(Z)-7-(tetrahydro-pyran-2-yloxy)-hept-3-ene-1,5-diynyl]-cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150637-64-2

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150637-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150637-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,3 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 150637-64:
(8*1)+(7*5)+(6*0)+(5*6)+(4*3)+(3*7)+(2*6)+(1*4)=122
122 % 10 = 2
So 150637-64-2 is a valid CAS Registry Number.

150637-64-2Relevant academic research and scientific papers

Synthesis of a protected (±)-calicheamicinone derivative by sequential introduction of functionality into the bicyclo[7.3.1]enediyne core structure

Magnus, Philip,Miknis, Gregory F.,Press, Neil J.,Grandjean, Didier,Taylor, G. Mark,Harling, John

, p. 6739 - 6748 (2007/10/03)

The core bicyclo[7.3.0]enediyne 3 has been synthesized from the protected cyclohexane-1,2-dione 6 and enediyne component 9. Conversion of 20 into more highly functionalized enediynes was accomplished by oxidation and amination to give 27. ProteCtion of 27

A general strategy using η2Co2(CO)6 acetylene complexes for the synthesis of the enediyne antitumor agents esperamicin, calicheamicin, dynemicin and neocarzinostatin

Magnus

, p. 1397 - 1418 (2007/10/02)

A review of the use of η2Co2(CO)6-acetylene complexes as stable intermediates for the construction of the core structures of the antitumor enediyne agent esperamicin, calicheamicin, dynemicin and neocarzinostatin from the

Conjugate addition-aldol approach to the simple bicyclic-diynene core structure found in the esperamicins and calicheamicins

Kadow, John F.,Tun, Min Min,Vyas, Dolatrai M.,Wittman, Mark D.,Doyle, Terrence W.

, p. 1423 - 1426 (2007/10/02)

The stable 12-β-hydroxybicyclo[7.1.0] diynene core 15 has been prepared stereospecifically. The key step consists of conjugate addition of dimethylaluminum benzenethiolate to enone aldehyde 12 followed by an in situ titanium isopropoxide assisted aldol cy

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