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1-allyl-4-hydroxy-1H-quinolinone is a chemical compound with the molecular formula C14H11NO2. It is a derivative of quinolinone, a heterocyclic compound with a quinoline ring structure and a ketone functional group. The compound features a hydroxyl group at the 4-position and an allyl group at the 1-position, which contributes to its unique chemical properties. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of dyes and pigments. Due to its complex structure and functional groups, 1-allyl-4-hydroxy-1H-quinolinone is a subject of interest in organic chemistry research, with potential implications in the development of new materials and compounds with specific properties.

1464-30-8

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1464-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1464-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1464-30:
(6*1)+(5*4)+(4*6)+(3*4)+(2*3)+(1*0)=68
68 % 10 = 8
So 1464-30-8 is a valid CAS Registry Number.

1464-30-8Downstream Products

1464-30-8Relevant academic research and scientific papers

4-hydroxy-2-quinolones 172*. Synthesis and structure of 4,3′-spiro[(6-allyl-2-amino- 5-oxo-5,6-dihydro-4h-pyrano- [3,2-c]quinoline-3-carbo- nitrile)-2′-oxindole]

Ukrainets,Red’kin,Sidorenko,Turov

, p. 1478 - 1484 (2009)

A three-component condensation of 1-allyl-4-hydroxy-2-oxo-1,2- dihydroquinoline, isatin, and malononitrile gave a satisfactory yield of 4,3′-spiro[(6-allyl-2-amino-5-oxo-5,6-dihydro-4H-pyrano-[3,2-c] quinoline-3-carbonitrile)-2′-oxindole], which structure was confirmed by X-ray analysis.

4-Hydroxy-2-quinolinones 128. Bromination of N-allyl-4-hydroxy-2-oxo-1,2- dihydroquinolines and pyridines unsubstituted in position 3

Ukrainets,Bereznyakova,Turov,Slobodzian

, p. 1159 - 1166 (2007)

Bromination of N-allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline and N-allyl-5-ethoxycarbonyl-4-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine is accompanied not only by closing of a five membered oxazole ring but also by a second bromination of the 2-bromomethyl-5-oxo-1,2-dihydro-5H-oxazolo[3,2-a]- derivatives formed at position 4.

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