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1H-Phenalen-1-one, 9-(3,4-dihydroxyphenyl)-2-hydroxy- is a complex organic compound with the molecular formula C19H12O5. It is a derivative of phenalen-1-one, featuring a 3,4-dihydroxyphenyl group at the 9-position and a hydroxyl group at the 2-position. 1H-Phenalen-1-one, 9-(3,4-dihydroxyphenyl)-2-hydroxy- is characterized by its tricyclic structure, with two benzene rings fused to a cyclohexenone ring. It exhibits a range of chemical properties, including reactivity towards electrophilic substitution due to the presence of the phenolic hydroxyl groups. The compound may have potential applications in the synthesis of pharmaceuticals, dyes, or other organic materials, given its unique structure and functional groups. However, further research and characterization are needed to fully understand its properties and potential uses.

56252-03-0

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56252-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56252-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,5 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56252-03:
(7*5)+(6*6)+(5*2)+(4*5)+(3*2)+(2*0)+(1*3)=110
110 % 10 = 0
So 56252-03-0 is a valid CAS Registry Number.

56252-03-0Upstream product

56252-03-0Relevant academic research and scientific papers

Variability of phenylpropanoid precursors in the biosynthesis of phenylphenalenones in Anigozanthos preissii

Schmitt, Bettina,Hoelscher, Dirk,Schneider, Bernd

, p. 331 - 337 (2000)

Feeding experiments using 13C labelled precursors and NMR spectroscopic studies revealed general biosynthetic incorporation of phenylalanine and variable incorporation of cinnamic acid, p-coumaric acid, caffeic acid and ferulic acid into phenylphenalenones in root cultures of Anigozanthos preissii. Evidence was obtained for parallel pathways of phenylphenalenone biosynthesis, with respect to the left phenylpropanoid unit, and a sequence involving utilisation of p-coumaric acid with late generation of an intermediate catechol moiety in the right phenylpropanoid unit. (C) 2000 Elsevier Science Ltd.

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