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4-Methyl-1-phenylquinolin-2(1H)-one is a chemical compound with the molecular formula C16H13NO. It belongs to the class of organic compounds known as quinolinones, which are characterized by a quinoline bearing a carbonyl group. These compounds have a characteristic bitter taste and are pale yellow in color. They are used in the preparation of various other compounds, often acting as an intermediate in the preparation of more complex molecules. They demonstrate various biological activities, although their potential for therapeutic or industrial applications largely depends on their specific chemical structures. Like all chemicals, they should be handled carefully to prevent unwanted reactions or harm.

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  • 2540-30-9 Structure
  • Basic information

    1. Product Name: 4-Methyl-1-phenylquinolin-2(1H)-one
    2. Synonyms: 4-Methyl-1-phenylquinolin-2(1H)-one;4-METHYL-1-PHENYL-2(1H)-QUINOLONE;4-methyl-1-phenyl-2(1H)-Quinolinone;4-Methyl-1-phenyl-quinolin-2-one
    3. CAS NO:2540-30-9
    4. Molecular Formula: C16H13NO
    5. Molecular Weight: 235.28052
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 2540-30-9.mol
  • Chemical Properties

    1. Melting Point: 134-135 °C
    2. Boiling Point: 386°Cat760mmHg
    3. Flash Point: 179.6°C
    4. Appearance: /
    5. Density: 1.18g/cm3
    6. Vapor Pressure: 3.64E-06mmHg at 25°C
    7. Refractive Index: 1.629
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: -3.47±0.40(Predicted)
    11. CAS DataBase Reference: 4-Methyl-1-phenylquinolin-2(1H)-one(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-Methyl-1-phenylquinolin-2(1H)-one(2540-30-9)
    13. EPA Substance Registry System: 4-Methyl-1-phenylquinolin-2(1H)-one(2540-30-9)
  • 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: 2540-30-9(Hazardous Substances Data)

2540-30-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Methyl-1-phenylquinolin-2(1H)-one is used as an intermediate compound for the synthesis of more complex molecules, particularly in the development of new drugs. Its presence in the molecular structure can contribute to the biological activity of the final product, making it a valuable component in the pharmaceutical industry.
Used in Chemical Research:
4-Methyl-1-phenylquinolin-2(1H)-one is used as a research compound in the field of organic chemistry. It serves as a model for understanding the properties and reactivity of quinolinones, which can help in the design and synthesis of new compounds with potential applications in various industries.
Used in Industrial Applications:
4-Methyl-1-phenylquinolin-2(1H)-one is used as a building block in the preparation of various industrial chemicals. Its versatility in forming different molecular structures allows it to be a key component in the production of dyes, pigments, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 2540-30-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2540-30:
(6*2)+(5*5)+(4*4)+(3*0)+(2*3)+(1*0)=59
59 % 10 = 9
So 2540-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H13NO/c1-12-11-16(18)17(13-7-3-2-4-8-13)15-10-6-5-9-14(12)15/h2-11H,1H3

2540-30-9SDS

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 4-methyl-1-phenylquinolin-2-one

1.2 Other means of identification

Product number -
Other names 4-Methyl-1-phenyl-1H-chinolin-2-on

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:2540-30-9 SDS

2540-30-9Relevant articles and documents

Nucleic acid fluorescent dye as well as preparation and application thereof

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Paragraph 0058; 0062-0063, (2021/11/03)

The invention relates to the field of fluorescent dyes, in particular to a novel nucleic acid fluorescent dye. The invention provides a fluorescent dye, and the structural formula of the fluorescent dye is as shown in formula I, wherein A is chloride

Novel intercalating fluorescent dyes for labelling nucleic acids and the preparation method thereof

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Paragraph 0073-0075, (2021/03/30)

The novel intercalating fluorescent compounds of exemplary embodiments of the present invention for analyzing nucleic acids, etc. have excellent intercalating efficiency with nucleic acids such as DNA and RNA of biomaterials, and may not only continuously

Novel fluorescent dye as well as preparation method and application thereof

-

Paragraph 0040; 0044-0045; 0050; 0054-0055, (2020/07/15)

The invention belongs to the technical field of fluorescent dyes, and provides a novel fluorescent dye which has the following structural general formula I defined in the specification. A preparationmethod of the novel fluorescent dye comprises the follow

Visible-Light-Photocatalyzed Synthesis of Phenanthridinones and Quinolinones via Direct Oxidative C-H Amidation

Moon, Yonghoon,Jang, Eunyoung,Choi, Soyeon,Hong, Sungwoo

supporting information, p. 240 - 243 (2018/01/17)

A straightforward synthetic strategy to construct biologically relevant phenanthridinones and quinolinones was developed via visible-light-promoted direct oxidative C-H amidation. In this photocatalytic system, amidyl radicals can be generated by homolysis of the N-H bond of simple amide precursors via single-electron transfer under blue LED illumination, which leads to oxidative intramolecular C-H amidation. Moreover, an efficient synthetic strategy using a photocascade enabled facile assembly of quinolinone structures through a catalytic sequence involving triplet energy (ET) transfer-based E/Z olefin isomerization and subsequent photocatalytic generation of amidyl radical intermediates.

Metal-free regioselective formation of C-N and C-O bonds with the utilization of diaryliodonium salts in water: Facile synthesis of: N-Arylquinolones and aryloxyquinolines

Mehra, Manish Kumar,Tantak, Mukund P.,Arun,Kumar, Indresh,Kumar, Dalip

supporting information, p. 4956 - 4961 (2017/07/10)

Regioselective construction of crucial C-N and C-O bonds leading to N-Arylquinolones and aryloxyquinolines has been accomplished by employing easily accessible diaryliodonium salts and quinolones in water under metal-and ligand-free conditions. This opera

Palladium-catalyzed [3+3] annulation between diarylamines and α,β-unsaturated acids through C-H activation: Direct access to 4-substituted 2-quinolinones

Kancherla, Rajesh,Naveen, Togati,Maiti, Debabrata

supporting information, p. 8360 - 8364 (2015/06/02)

A C-H activation strategy has been successfully employed for the high-yielding synthesis of a diverse array of 4-substituted 2-quinolinone species by a palladium-catalyzed dehydrogenative coupling involving diarylamines. This intermolecular annulation app

Method for optical measurement of multi-stranded nucleic acid using cyanine dyes

-

, (2008/06/13)

A method for optical measurement of a multi-stranded nucleic acid which comprises the step of bringing a compound into contact with a multi-stranded nucleic acid wherein said compound is capable of interacting with the multi-stranded nucleic acid, wherein the compound has the following properties:(a) the compound can exist in a substantially colorless and non-fluorescent state under at least one condition in an aqueous solution in the absence of the multi-stranded nucleic acid, and(b) when the multi-stranded nucleic acid is allowed to exist in the condition defined in the above (a), the compound changes to a substantially colored state based on an interaction with the multi-stranded nucleic acid and substantially expresses fluorescent property based on said interaction.

Substituted unsymmetrical cyanine dyes with selected permeability

-

, (2008/06/13)

The invention describes the preparation and use of fluorescent stains for nucleic acids derived from unsymmetrical cyanine dyes comprising a substituted benzazolium ring system linked by a methine bridge to a pyridinium or quinolinium ring system having at least one substituent on the pyridinium or quinolinium ring that contains a heteroatom. The presence of the heteroatom-containing substituent results in higher sensitivity to oligonucleotides and larger nucleic acid polymers in a wide range of cells and gels, and for use in analysis of cell structure, membrane integrity or function.

Fluorescent assay for bacterial gram reaction

-

, (2008/06/13)

The invention relates to a method of analyzing a sample thought to contain bacteria using an aqueous solution comprising one or more fluorescent dyes: a fluorescent dye of formula I, a fluorescent dye of formula II, a fluorescent dye of formula III, and a

Cyclic-substituted unsymmetrical cyanine dyes

-

, (2008/06/13)

The invention describes the preparation and use of fluorescent stains for nucleic acids derived from unsymmetrical cyanine dyes. In particular, the invention describes unsymmetrical cyanine dyes having a saturated or unsaturated cyclic substituent. The dyes of the invention possess superior fluorescent characteristics when complexed with nucleic acids, and have utility in any application which requires detection of nucleic acids. The presence of the cyclic substituent results in improved permeability in a wide range of living cells, resulting in improved detection of intracellular nucleic acids.

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