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β-Phenyl-β-propiolactone is a chemical compound with the molecular formula C9H8O2. It is a cyclic ester derived from phenylacetaldehyde, featuring a phenyl group attached to a β-propiolactone ring. This lactone is known for its reactivity and is used as a synthetic intermediate in the preparation of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its ability to form stable derivatives with amines, it is also employed in the synthesis of β-amino acids and other biologically active molecules. β-Phenyl-β-propiolactone is a colorless to pale yellow solid that is sensitive to light and moisture, and it is typically handled under controlled conditions to maintain its stability.

4287-98-3

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4287-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4287-98-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4287-98:
(6*4)+(5*2)+(4*8)+(3*7)+(2*9)+(1*8)=113
113 % 10 = 3
So 4287-98-3 is a valid CAS Registry Number.

4287-98-3Downstream Products

4287-98-3Relevant academic research and scientific papers

Cationic palladium(II) complex-catalyzed [2 + 2] cycloaddition and tandem cycloaddition-allylic rearrangement of ketene with aldehydes: An improved synthesis of sorbic acid

Hattori, Tetsutaro,Suzuki, Yutaka,Uesugi, Osamu,Oi, Shuichi,Miyano, Sotaro

, p. 73 - 74 (2000)

Cationic palladium(II) complexes [PdL2(PhCN)2](BF4)2 efficiently catalyze the [2 + 2] cycloaddition of ketene with aldehydes to give the corresponding oxetan-2-ones, among which 4-vinyl-substituted ones are further isomerized under the conditions to give 3,6-dihydro-2H-pyran-2-ones in good yields.

Asymmetric Cycloaddition of Ketene with Aldehydes catalysed by Chiral Bissulfonamide-Trialkylaluminium Complexes

Tamai, Yasufumi,Yoshiwara, Hideki,Someya, Masahiro,Fukumoto, Jun,Miyano, Sotaro

, p. 2281 - 2282 (2007/10/02)

Asymmetric cycloaddition of ketene with the aldehydes 1a-g, catalysed by 10 molpercent of C2-symmetric bissulfonamide 2a-c-R3Al complexes afforded optically active 4-substituted oxetan-2-ones 3a-g in up to 74percent enantiomeric excess.

THE REACTION OF SMALL RING COMPOUND WITH CARBON MONOXIDE. THE CARBONYLATION OF OXIRANE

Kamiya, Yoshio,Kawato, Katsuhito,Ohta, Hiroyuki

, p. 1549 - 1552 (2007/10/02)

The carbonylation of oxiranes catalyzed by rhodium complex afforded β-lactones.Various factors which control the above reaction are presented.

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