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128366-03-0

(3E)-3-[hydroxy(propylamino)methylidene]quinoline-2,4(1H,3H)-dione is a quinoline-2,4-dione derivative featuring a (3E)-3-[hydroxy(propylamino)methylidene] moiety. This organic compound has a molecular formula of C14H15N3O3 and a molecular weight of 273.29 g/mol. Its unique chemical structure and properties position it as a promising candidate for pharmaceutical applications and further research in medicinal chemistry.

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  • 128366-03-0 Structure

  • Basic information

    1. Product Name: (3E)-3-[hydroxy(propylamino)methylidene]quinoline-2,4(1H,3H)-dione
    2. Synonyms:
    3. CAS NO:128366-03-0
    4. Molecular Formula: C13H14N2O3
    5. Molecular Weight: 246.2619
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128366-03-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 439.8°C at 760 mmHg
    3. Flash Point: 219.8°C
    4. Appearance: N/A
    5. Density: 1.296g/cm3
    6. Vapor Pressure: 1.64E-08mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3E)-3-[hydroxy(propylamino)methylidene]quinoline-2,4(1H,3H)-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3E)-3-[hydroxy(propylamino)methylidene]quinoline-2,4(1H,3H)-dione(128366-03-0)
    12. EPA Substance Registry System: (3E)-3-[hydroxy(propylamino)methylidene]quinoline-2,4(1H,3H)-dione(128366-03-0)

  • 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: 128366-03-0(Hazardous Substances Data)

128366-03-0 Usage

Uses

Used in Pharmaceutical Industry:
(3E)-3-[hydroxy(propylamino)methylidene]quinoline-2,4(1H,3H)-dione is utilized as a potential drug candidate for a variety of therapeutic applications. Its specific chemical structure and properties make it a valuable compound for exploration and development in the field of medicinal chemistry, with the aim of discovering new treatments and therapies for various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 128366-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,6 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128366-03:
(8*1)+(7*2)+(6*8)+(5*3)+(4*6)+(3*6)+(2*0)+(1*3)=130
130 % 10 = 0
So 128366-03-0 is a valid CAS Registry Number.

128366-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-2-oxo-N-propyl-1H-quinoline-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-Quinolinecarboxamide,1,2-dihydro-4-hydroxy-2-oxo-N-propyl

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:128366-03-0 SDS

128366-03-0Downstream Products

128366-03-0Relevant articles and documents

4-Hydroxy-2-quinolones. 93. Synthesis and biological properties of 2-hydroxy-4-imino-1,4-dihydroquinoline-3-carboxylic acid N-R-amides

Ukrainets,Sidorenko,Gorokhova,Jaradat

, p. 475 - 487 (2008/02/02)

Various methods of synthesizing amides of 2-hydroxy-4-imino-1,4- dihydroquinoline-3-carboxylic acids have been studied. Results of investigations on the antitubercular and antiinflammatory activity of the obtained compounds are discussed. 2006 Springer Sc

4-Hydroxy-2-quinolones. 4. Selection of the Optimum Path for the Synthesis of N-R-Substituted 4-Hydroxy-2-quinolone-3-carboxylic Acid Amides

Ukrainets, I. V.,Bezuglyi, P. A.,Treskach, V. I.,Turov, A. V.

, p. 538 - 540 (2007/10/02)

A comparison of several methods of preparation of N-R-substituted 4-hydroxy-2-quinolone-3-carboxylic acid amides showed that intramolecular cyclization of 2-carbalkoxymalonanilic acid ethyl esters with simultaneous amidation is the most rational method.

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