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1-Phenylhex-5-en-2-yn-1-one is an organic compound characterized by a unique molecular structure that features a phenyl group (a benzene ring) attached to a hex-5-en-2-yn-1-one backbone. This backbone consists of a hexane chain with a triple bond between the second and third carbon atoms, and a double bond between the fifth and sixth carbon atoms. The presence of both a triple bond and a double bond in the molecule endows it with interesting chemical reactivity and potential applications in the synthesis of various organic compounds. The compound's molecular formula is C12H10O, reflecting its composition of 12 carbon atoms, 10 hydrogen atoms, and 1 oxygen atom. Due to its structural features, 1-phenylhex-5-en-2-yn-1-one can be involved in a range of chemical reactions, such as addition reactions across the triple bond, and may be used as a building block in the preparation of more complex molecules in organic chemistry.

829-56-1

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829-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 829-56-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 829-56:
(5*8)+(4*2)+(3*9)+(2*5)+(1*6)=91
91 % 10 = 1
So 829-56-1 is a valid CAS Registry Number.

829-56-1Relevant academic research and scientific papers

Efficient methods of synthesis of unsaturated alcohols and ketones by allylation of Favorsky reaction products under phase transfer conditions

Potapov,Yaroshenko,Panov,Musalov,Khabibulina,Musalova,Amosova

, p. 1733 - 1737 (2016)

Allylation of the Favorsky reaction products with allyl halides under phase-transfer catalysis in the system CuI–K2CO3–Na2SO3–BTEAC–H2O–C6H6afforded the corresponding allylpropar

Bronsted acid catalyzed cycloisomerizations of 5,2-enyne-1-ones: Highly regioselective synthesis of 2,3-dihydro-4H-pyran-4-ones

Yang, Fang,Ji, Ke-Gong,Zhao, Shu-Chun,Ali, Shaukat,Ye, Yu-Ying,Liu, Xue-Yuan,Liang, Yong-Min

supporting information; experimental part, p. 6470 - 6474 (2012/06/15)

Dual-action catalyst: A Bronsted acid catalyzed regioselective cycloisomerization was found to be highly effective for the preparation of structurally diverse 2,3-dihydro-4H-pyran-4-ones in a 6-exo-trig manner from the corresponding 5,2-enyne-1-ones. In t

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