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CAS

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1614221-79-2

3,3-dibenzyl-4-hydroxy-8-methoxy-3,4-dihydro-1H-quinolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1614221-79-2 Structure

  • Basic information

    1. Product Name: 3,3-dibenzyl-4-hydroxy-8-methoxy-3,4-dihydro-1H-quinolin-2-one
    2. Synonyms: 3,3-dibenzyl-4-hydroxy-8-methoxy-3,4-dihydro-1H-quinolin-2-one
    3. CAS NO:1614221-79-2
    4. Molecular Formula:
    5. Molecular Weight: 373.452
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1614221-79-2.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: 3,3-dibenzyl-4-hydroxy-8-methoxy-3,4-dihydro-1H-quinolin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3-dibenzyl-4-hydroxy-8-methoxy-3,4-dihydro-1H-quinolin-2-one(1614221-79-2)
    11. EPA Substance Registry System: 3,3-dibenzyl-4-hydroxy-8-methoxy-3,4-dihydro-1H-quinolin-2-one(1614221-79-2)

  • 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: 1614221-79-2(Hazardous Substances Data)

1614221-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1614221-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,4,2,2 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1614221-79:
(9*1)+(8*6)+(7*1)+(6*4)+(5*2)+(4*2)+(3*1)+(2*7)+(1*9)=132
132 % 10 = 2
So 1614221-79-2 is a valid CAS Registry Number.

1614221-79-2Downstream Products

1614221-79-2Relevant articles and documents

Synthesis of symmetrically substituted 3,3-dibenzyl-4-hydroxy-3,4-dihydro- 1H-quinolin-2-ones, as novel quinoline derivatives with antibacterial activity

Ferretti, Matías D.,Neto, Alexandre T.,Morel, Ademir F.,Kaufman, Teodoro S.,Larghi, Enrique L.

, p. 253 - 266 (2014/06/09)

A novel series of symmetrically substituted 3,3-dibenzyl-4-hydroxy-3,4- dihydro-1H-quinolin-2-ones was synthesized and tested as antimicrobials. The minimum inhibitory concentration (MIC) values of the most active heterocycles were slightly higher than those exhibited by levofloxacin, employed as comparator. Structural factors affecting the activity were explored along three diversification points, including the substituents of the aromatic rings of the 3-benzyl moieties, as well as the functionalization of both, the homocyclic ring of the heterocycle and the quinolonic nitrogen atom. 6-Chloro and 3,3-bis(4′-chlorobenzyl) derivatives showed the lower MIC values. Optimally substituted heterocycles were synthesized, which exhibited enhanced activity.

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