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173544-82-6

2-oxo-2-phenylethyl 2-(methylamino)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 173544-82-6 Structure

  • Basic information

    1. Product Name: 2-oxo-2-phenylethyl 2-(methylamino)benzoate
    2. Synonyms: 2-oxo-2-phenylethyl 2-(methylamino)benzoate
    3. CAS NO:173544-82-6
    4. Molecular Formula: C16H15NO3
    5. Molecular Weight: 269.2952
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 173544-82-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    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: 2-oxo-2-phenylethyl 2-(methylamino)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-oxo-2-phenylethyl 2-(methylamino)benzoate(173544-82-6)
    11. EPA Substance Registry System: 2-oxo-2-phenylethyl 2-(methylamino)benzoate(173544-82-6)

  • 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: 173544-82-6(Hazardous Substances Data)

173544-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173544-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,5,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 173544-82:
(8*1)+(7*7)+(6*3)+(5*5)+(4*4)+(3*4)+(2*8)+(1*2)=146
146 % 10 = 6
So 173544-82-6 is a valid CAS Registry Number.

173544-82-6Relevant articles and documents

2-Aryl-3-hydroxyquinolones, a new class of dyes with solvent dependent dual emission due to excited state intramolecular proton transfer

Yushchenko, Dmytro A.,Shvadchak, Volodymyr V.,Klymchenko, Andrey S.,Duportail, Guy,Mely, Yves,Pivovarenko, Vasyl G.

, p. 774 - 781 (2007/10/03)

Herein, the fluorescence properties of a series of 2-aryl-3- hydroxyquinolones (3HQs) were investigated and compared with the properties of well-studied 3-hydroxyflavone. All these compounds were found to display dual fluorescence with well-separated band

Preparation of 1,2-disubstituted-3-hydroxy-4(1H)-quinolinones and the influence of substitution on the course of cyclization

Hradil, Pavel,Hlavac, Jan,Lemr, Karel

, p. 141 - 144 (2007/10/03)

Synthesis of 1,2-disubstituted-3-hydroxy-4(1H)-quinolinones by the cyclization of N-substituted phenacyl or acetonyl anthranilates is described. Two methods were employed for cyclization of anthranilates. Heating in polyphosphoric acid has a wide scope of applicability. The thermal cyclization in boiling N-methylpyrrolidone is limited by steric effect.

Synthetic Routes to 1,5-Dihydro-5-oxo-4,1-benzoxazepines and to 5-Oxooxazoloquinolines

Gandhi, Sham S.,Bell, Karen L.,Gibson, Martin S.

, p. 13301 - 13308 (2007/10/02)

The literature concerning phenacyl anthranilate, N-phenacylanthranilic acid and phenacyl N-phenacylanthranilate is clarified.Phenacyl anthranilate is dehydrated to 1,5-dihydro-5-oxo-2-phenyl-4,1-benzoxazepine by treatment with phosphoryl chloride; other examples of this reaction are described.A preparation of 4-methyl-5-oxo-2-phenyloxazoloquinoline from N-phenacylanthranilic acid and propionic anhydride is reported.

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