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2554-84-9

2-(2,3-dimethoxyphenyl)-4H-chromen-4-one is a complex organic compound with the molecular formula C17H14O5. It is a derivative of the flavone class of flavonoids, characterized by a benzopyrone structure with a phenyl ring attached at the 2-position. 2-(2,3-dimethoxyphenyl)-4H-chromen-4-one features two methoxy groups at the 2 and 3 positions of the phenyl ring, contributing to its chemical properties. It is known for its potential antioxidant and anti-inflammatory activities, which are being studied for their implications in various biological and medicinal applications. The compound's structure endows it with unique pharmacological properties, making it a subject of interest in the field of natural product chemistry and drug development.

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  • 2554-84-9 Structure

  • Basic information

    1. Product Name: 2-(2,3-dimethoxyphenyl)-4H-chromen-4-one
    2. Synonyms: 2-(2,3-Dimethoxyphenyl)-4H-chromen-4-one; 2',3'-Dimethoxyflavone; 2554-84-9
    3. CAS NO:2554-84-9
    4. Molecular Formula: C17H14O4
    5. Molecular Weight: 282.2907
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2554-84-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 436.9°C at 760 mmHg
    3. Flash Point: 194.7°C
    4. Appearance: N/A
    5. Density: 1.242g/cm3
    6. Vapor Pressure: 7.83E-08mmHg at 25°C
    7. Refractive Index: 1.598
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(2,3-dimethoxyphenyl)-4H-chromen-4-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(2,3-dimethoxyphenyl)-4H-chromen-4-one(2554-84-9)
    12. EPA Substance Registry System: 2-(2,3-dimethoxyphenyl)-4H-chromen-4-one(2554-84-9)

  • 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: 2554-84-9(Hazardous Substances Data)

2554-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2554-84-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2554-84:
(6*2)+(5*5)+(4*5)+(3*4)+(2*8)+(1*4)=89
89 % 10 = 9
So 2554-84-9 is a valid CAS Registry Number.

2554-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,3-dimethoxyphenyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 2-(2,3-dimethoxy-phenyl)-chromen-4-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:2554-84-9 SDS

2554-84-9Relevant articles and documents

Ortho Substituent Effect of the Side-Chain Phenyl Group on the Dehydrogenation of Flavanones with 2,3-Dichloro-5,6-dicyano-p-benzoquinone

Hoshino, Yukio,Takeno, Noboru

, p. 4468 - 4470 (2007/10/02)

Rates of the dehydrogenation of 2'-substituted flavanones with 2,3-dichloro-5,6-dicyano-p-benzoquinone were measured by means of HPLC analyses.All substituents at the ortho position of the side-chain phenyl group of flavanones showed a retarding effect on the reaction.A correlation analysis for the ortho effect using the linear combination model has led to a conclusion that the inductive effect is much more important than the steric and the resonance effect, and that the steric effect is slightly greater than the resonance effect.

Cyclodehydrogenation of 2'-Hydroxychalcones with DDQ: A Simple Route for Flavones and Aurones

Imafuku, Kimiaki,Honda, Masaaki,McOmie, J. F. W.

, p. 199 - 201 (2007/10/02)

The oxidation of 2'-hydroxychalcones with 2,3-dichloro-5,6-dicyano-p-benzoquinone provides a useful synthetic route for flavones and aurones.

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