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[(2S,3R)-3-((1S,2R)-1,2-Bis-benzyloxy-but-3-enyl)-oxiranyl]-(2,3-dihydro-indol-1-yl)-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

847779-86-6

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847779-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 847779-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,7,7 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 847779-86:
(8*8)+(7*4)+(6*7)+(5*7)+(4*7)+(3*9)+(2*8)+(1*6)=246
246 % 10 = 6
So 847779-86-6 is a valid CAS Registry Number.

847779-86-6Downstream Products

847779-86-6Relevant academic research and scientific papers

A diversity-oriented synthetic approach to bengamides

Sarabia, Francisco,Sánchez-Ruiz, Antonio

, p. 1131 - 1135 (2005)

A new approach to the bengamides, a new class of antitumor natural products of marine origin, is reported from epoxyamides, prepared by reaction of aldehydes with sulfur ylides. The synthetic strategy has been designed for the delivery of a wide array of

Chiral sulfur ylides for the synthesis of bengamide e and analogues

Sarabia, Francisco,Martin-Galvez, Francisca,Chammaa, Samy,Martin-Ortiz, Laura,Sanchez-Ruiz, Antonio

supporting information; experimental part, p. 5526 - 5532 (2010/11/17)

A new synthetic methodology of asymmetric epoxidation developed in our laboratories has been employed for the stereoselective synthesis of bengamide E (16) and analogues at the terminal olefinic position. In the event, the chiral sulfonium salt 30 was transformed into its corresponding sulfur ylide and reacted with aldehydes 21 and 44 to efficiently provide epoxy amides 31 and 45, respectively. To access the bengamides from these epoxy amides, we combined a synthetic strategy previously reported by us, using an olefin cross metathesis reaction to introduce various alkyl substituents at the terminal olefinic position of amide 33, with reactions mediated by palladium (Negishi or Suzuki couplings) from amide 49. This latter route of introduction of alkyl groups proved to be more efficient than the metathesis approach and allowed access to the generation of a wide array of new bengamide analogues.

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