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1-Furan-2-yl-but-2-yn-1-one is an organic compound characterized by a unique structure that combines a furan ring with a butyn-1-one moiety. This molecule features a furan ring, which is a five-membered aromatic ring containing one oxygen atom, and a butyn-1-one group, which is a four-carbon chain with a triple bond at the second carbon and a carbonyl group at the first carbon. The compound is known for its distinct chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Due to its specific structure, 1-furan-2-yl-but-2-yn-1-one can participate in a range of chemical reactions, making it a valuable building block for the synthesis of more complex molecules.

39659-06-8

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39659-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39659-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39659-06:
(7*3)+(6*9)+(5*6)+(4*5)+(3*9)+(2*0)+(1*6)=158
158 % 10 = 8
So 39659-06-8 is a valid CAS Registry Number.

39659-06-8Downstream Products

39659-06-8Relevant academic research and scientific papers

Phosphonium Salts and Phosphoranes. Part 5. Thermal and Electron-Impact Induced Fragmentation of Heteroaroylmethylenetriphenylphosphoranes.

Brittain, Judith M.,Jones, R. Alan,Taheri, Sayed Ali Naghi

, p. 7609 - 7618 (1992)

A modification of Trippett's pyrolysis of aroylmethylenephosphoranes provides a general procedure for the synthesis of five-membered heteroarylethynes.The electron-impact induced fragmentation of the phosphoranes also produced ions corresponding in mass to the ethynes, but metastable ion data indicate that the extrusion of the ethyne follows the initial loss of H* from the molecular ion.

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