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5614-80-2

Ethyl 2-((2-oxo-4-phenyl-2H-chromen-7-yl)oxy)acetate is a complex organic compound with the molecular formula C18H14O5. It is a derivative of the naturally occurring flavonoid, 2-oxo-4-phenyl-2H-chromen-7-yl, which is known for its antioxidant properties. This specific compound features an ethyl group attached to a 2-oxo-4-phenyl-2H-chromen-7-yl moiety through an acetate linkage. It is characterized by its potential applications in pharmaceuticals and as a chemical intermediate in the synthesis of various biologically active compounds. The compound's structure and properties make it a subject of interest in the field of organic chemistry, particularly for its potential roles in drug development and the creation of new materials with specific therapeutic or industrial applications.

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  • 5614-80-2 Structure

  • Basic information

    1. Product Name: ethyl 2-((2-oxo-4-phenyl-2H-chromen-7-yl)oxy)acetate
    2. Synonyms: ethyl 2-((2-oxo-4-phenyl-2H-chromen-7-yl)oxy)acetate
    3. CAS NO:5614-80-2
    4. Molecular Formula:
    5. Molecular Weight: 324.333
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5614-80-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl 2-((2-oxo-4-phenyl-2H-chromen-7-yl)oxy)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-((2-oxo-4-phenyl-2H-chromen-7-yl)oxy)acetate(5614-80-2)
    11. EPA Substance Registry System: ethyl 2-((2-oxo-4-phenyl-2H-chromen-7-yl)oxy)acetate(5614-80-2)

  • 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: 5614-80-2(Hazardous Substances Data)

5614-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5614-80-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5614-80:
(6*5)+(5*6)+(4*1)+(3*4)+(2*8)+(1*0)=92
92 % 10 = 2
So 5614-80-2 is a valid CAS Registry Number.

5614-80-2Relevant articles and documents

Synthesis and biological evaluation of novel 7-hydroxy-4-phenylchromen-2-one–linked to triazole moieties as potent cytotoxic agents

Liu, Chuan-Feng,Shen, Qing-Kun,Li, Jia-Jun,Tian, Yu-Shun,Quan, Zheshan

, p. 1111 - 1119 (2017)

A new series of novel 7-hydroxy-4-phenylchromen-2-one (1a)–linked 1,2,4-triazoles were synthesised using a click chemistry approach. All derivatives were subjected to 3-(4,5-dimethylthiazol-yl)-diphenyl tetrazolium bromide (MTT) cytotoxicity screening aga

Synthesis and antimicrobial assessment of novel coumarins featuring 1,2,4-oxadiazole

Krishna, Challa,Bhargavi, M. Vijaya,Rao, Ch. Prasad,Krupadanam, G. L. David

, p. 3743 - 3751 (2015)

Oxadiazoles are heterocyclic compounds with a variety of application in many pharmaceuticals and agrochemical products. We report herein the convenient synthesis of 4-[(3-aryl-1,2,4-oxadiazol-5-yl)methoxy]-coumarins (4a-f), 6-[(3-aryl-1,2,4-oxadiazol-5-yl

New 4-phenylcoumarin derivatives as potent 3C protease inhibitors: Design, synthesis, anti-HAV effect and molecular modeling

Kassem, Asmaa F.,Batran, Rasha Z.,Abbas, Eman M.H.,Elseginy, Samia A.,Shaheen, Mohamed N.F.,Elmahdy, Elmahdy M.

, p. 447 - 460 (2019/03/07)

A new series of 4-phenylcoumarin derivatives was synthesized starting from (2-oxo-4-phenyl-2H-chromen-7-yloxy) acetic acid hydrazide 3. Evaluation of the target compounds for their antiviral activity against hepatitis A virus revealed that the ethylthiose

Synthesis of amino acid derivatives of 7-methoxycarbonylneoflavones

Garazd,Garazd,Smirnov,Khilya

, p. 415 - 419 (2007/10/03)

A number of aminoacyl derivatives of 4-phenylcoumarin have been obtained by the condensation of N-hydroxysuccinimide esters of 7-(1-carboxyalkoxy)-4-phenylcoumarins with L-amino acids and their derivatives.

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