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56252-02-9

Hydroxyanigorufone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56252-02-9 Structure

  • Basic information

    1. Product Name: Hydroxyanigorufone
    2. Synonyms: Hydroxyanigorufone;2-Hydroxy-9-(4-hydroxyphenyl)-1H-phenalen-1-one;Emenolone
    3. CAS NO:56252-02-9
    4. Molecular Formula: C19H12O3
    5. Molecular Weight: 288.29678
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56252-02-9.mol

  • Chemical Properties

    1. Melting Point: 201-204℃
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Hydroxyanigorufone(CAS DataBase Reference)
    10. NIST Chemistry Reference: Hydroxyanigorufone(56252-02-9)
    11. EPA Substance Registry System: Hydroxyanigorufone(56252-02-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 56252-02-9(Hazardous Substances Data)

56252-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56252-02-9 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 56252-02:
(7*5)+(6*6)+(5*2)+(4*5)+(3*2)+(2*0)+(1*2)=109
109 % 10 = 9
So 56252-02-9 is a valid CAS Registry Number.

56252-02-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name hydroxyanigorufone

1.2 Other means of identification

Product number -
Other names 2-hydroxy-9-(4-hydroxy-phenyl)-phenalen-1-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56252-02-9 SDS

56252-02-9Relevant articles and documents

Intermediates With Biosynthetic Implications In De Novo Production Of Phenyl-Phenalenone-Type Phytoalexins By Musa acuminata Revised Structure Of Emenolone

Luis, Javier G.,Fletcher, Winston Q.,Echeverri, Fernando,Grillo, Teresa A.,Perales, Aurea,Gonzalez, Jose A.

, p. 4117 - 4130 (1995)

Three new intermediates (1-3) in de novo biosynthetic pathway to phenyl-phenalenone-type phytoalexins have been isolated from rhizomes of Musa acuminata infected with the fungus Fusarium oxysporum.The structures of the new pre-phytoalexins were elucidated

Concise Synthesis of Natural Phenylphenalenone Phytoalexins and a Regioisomer

Wang, Ming-Zhong,Ku, Chuen-Fai,Si, Tong-Xu,Tsang, Siu-Wai,Lv, Xiao-Meng,Li, Xiao-Wan,Li, Zheng-Ming,Zhang, Hong-Jie,Chan, Albert S. C.

, p. 98 - 105 (2018/02/07)

Concise total syntheses of the natural phytoalexins 2-hydroxy-8-(4-hydroxyphenyl)phenalen-1-one (1), 2-hydroxy-8-(3,4-dihydroxyphenyl)phenalen-1-one (2), and hydroxyanigorufone (4), together with regioisomer 3 are accomplished in 11 or 12 steps. The synthetic strategy features a Friedel-Crafts acylation to construct the 1H-phenalen-1-one tricyclic core followed by a Suzuki cross-coupling to obtain the target compounds.

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

Schmitt, Bettina,Hoelscher, Dirk,Schneider, Bernd

, p. 331 - 337 (2007/10/03)

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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