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1-Phenyl-3-(2-furyl)prop-1-yne is an organic compound characterized by a unique molecular structure that features a propyne backbone, which is a three-carbon chain with a triple bond between the first and second carbon atoms. The first carbon is bonded to a phenyl group (a benzene ring), while the third carbon is connected to a furyl group (a five-membered ring with four carbon atoms and one oxygen atom). 1-phenyl-3-(2-furyl)prop-1-yne is known for its aromatic properties due to the presence of the phenyl and furyl rings, which contribute to its stability and reactivity. It is often used in the synthesis of various pharmaceuticals and other organic compounds due to its ability to form a variety of derivatives. The compound's molecular formula is C??H?O, reflecting its composition of 13 carbon atoms, 8 hydrogen atoms, and 1 oxygen atom.

4437-24-5

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4437-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4437-24-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4437-24:
(6*4)+(5*4)+(4*3)+(3*7)+(2*2)+(1*4)=85
85 % 10 = 5
So 4437-24-5 is a valid CAS Registry Number.

4437-24-5Downstream Products

4437-24-5Relevant academic research and scientific papers

Palladium-Catalyzed Decarboxylative Benzylation of Acetylides and Enolates

Torregrosa, Robert R. P.,Mendis, Shehani N.,Davies, Alex,Tunge, Jon A.

, p. 3205 - 3216 (2018/08/17)

Benzylic alkylation of enolates and acetylides has been achieved through the use of a decarboxylative benzylation strategy. Previous research in this area is often limited by the need for extended conjugation in the electrophiles that are coupled. Herein, we report that the use of 1,1'-bis(diphenylphosphino)ferrocene (dppf) ligand allows the coupling of simple benzyl electrophiles with enolates, while the use of XPhos ligand promotes the decarboxylative couplings of propiolates.

Lewis acid catalyzed propargylation of arenes with O-propargyl trichloroacetimidates: Synthesis of 1,3-diarylpropynes

Li, Changkun,Wang, Jianbo

, p. 7431 - 7434 (2008/02/11)

(Chemical Equation Presented) The BF3·OEt 2-catalyzed Friedel-Crafts propargylation of aromatic compounds with O-propargyl trichloroacetimidates is highly efficient and affords 1,3-diarylpropyne derivatives in good yields.

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