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3-Allyl-tetrahydropyran-2-one is a chemical compound with the molecular formula C8H12O2. It is a heterocyclic compound, specifically a derivative of tetrahydropyran, which is a saturated six-membered oxygen-containing ring. The compound features an allyl group (a propene unit) attached to the 3-position of the tetrahydropyran ring, and a ketone functional group at the 2-position. This organic compound is known for its unique chemical properties and can be used in various applications, such as a building block in the synthesis of more complex molecules or as an intermediate in the production of pharmaceuticals and fragrances. Its structure and reactivity make it an interesting target for organic chemists, who study its behavior in various reactions and potential applications in the chemical industry.

50994-84-8

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50994-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50994-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,9 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50994-84:
(7*5)+(6*0)+(5*9)+(4*9)+(3*4)+(2*8)+(1*4)=148
148 % 10 = 8
So 50994-84-8 is a valid CAS Registry Number.

50994-84-8Upstream product

50994-84-8Downstream Products

50994-84-8Relevant academic research and scientific papers

Calyciphylline B-Type Alkaloids: Total Syntheses of (-)-Daphlongamine H and (-)-Isodaphlongamine H

Hugelshofer, Cedric L.,Palani, Vignesh,Sarpong, Richmond

, p. 8431 - 8435 (2019)

The first total synthesis of the complex hexacylic Daphniphyllum alkaloid (-)-daphlongamine H has been accomplished. Key to the success of the strategy are a complexity-building Mannich reaction, efficient cyclizations, and a highly diastereoselective hydrogenation to assemble multigram quantities of the tricyclic core bearing four contiguous stereocenters. Following construction of the hydro-indene substructure by means of a Pauson-Khand reaction, endgame redox manipulations delivered the natural product. Importantly, the synthetic studies have also given access to (-)-isodaphlongamine H and led to a revision of the reported structure of deoxyisocalyciphylline B.

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