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(1R,3Z,7S,9E,11R,15S,17R)-11-hydroxy-7-{(1S,2E)-1-(4-methoxybenzyloxy)-3-[(2S)-4-methyl-3,6-dihydro-2H-pyran-2-yl]allyl}-15-methyl-13-methylene-6,21-dioxabicyclo[15.3.1]henicosa-3,9,19-trien-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1198463-35-2

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1198463-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198463-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,4,6 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1198463-35:
(9*1)+(8*1)+(7*9)+(6*8)+(5*4)+(4*6)+(3*3)+(2*3)+(1*5)=192
192 % 10 = 2
So 1198463-35-2 is a valid CAS Registry Number.

1198463-35-2Relevant academic research and scientific papers

Total synthesis of laulimalide: Assembly of the fragments and completion of the synthesis of the natural product and a potent analogue

Trost, Barry M.,Amans, Dominique,Seganish, W. Michael,Chung, Cheol K.

supporting information; experimental part, p. 2961 - 2971 (2012/04/23)

Herein, we present a full account of our efforts to couple the northern and the southern building blocks, the synthesis of which were described in the preceding paper, along with the modifications required to ultimately lead to a successful synthesis of laulimalide. Key highlights include an exceptionally efficient and atom-economical intramolecular ruthenium-catalyzed alkene-alkyne coupling to build the macrocycle, followed by a highly stereoselective 1,3-allylic isomerization promoted by a rhenium complex. Interestingly, the designed synthetic route also allowed us to prepare an analogue of the natural product that possesses significant cytotoxic activity. We also report a second generation route that provides a more concise synthesis of the natural product. All in one piece: Efforts to couple the northern and southern building blocks, synthesized in the preceding paper, along with modifications required to lead to a successful synthesis of laulimalide are discussed. Interestingly, the designed synthetic route also allowed the preparation of an analogue of the natural product that possesses significant cytotoxic activity (see scheme). A more concise, second-generation route to the natural product is also described. Copyright

Evaluating transition-metal-catalyzed transformations for the synthesis of laulimalide

Trost, Barry M.,Amans, Dominique,Seganish, W. Michael,Chung, Cheol K.

supporting information; experimental part, p. 17087 - 17089 (2010/03/23)

(Chemical Equation Presented) Laulimalide is a structurally unique 20-membered marine macrolide displaying microtubule stabilizing activity similar to that of paclitaxel and the epothilones. The use of atom-economical transformations such as a Rh-catalyze

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