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(3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione is a chemical compound with the molecular formula C18H20N2O3. It is a derivative of quinoline-2,4-dione and contains a butylamino group and a hydroxy methylidene group. (3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione has potential pharmacological properties and may be investigated for its therapeutic effects. It is important to handle this chemical with caution, as it may have specific health and environmental hazards associated with its use.

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  • 128366-05-2 Structure
  • Basic information

    1. Product Name: (3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione
    2. Synonyms:
    3. CAS NO:128366-05-2
    4. Molecular Formula: C14H16N2O3
    5. Molecular Weight: 260.2884
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128366-05-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 448.6°C at 760 mmHg
    3. Flash Point: 225.1°C
    4. Appearance: N/A
    5. Density: 1.26g/cm3
    6. Vapor Pressure: 7.83E-09mmHg at 25°C
    7. Refractive Index: 1.592
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione(128366-05-2)
    12. EPA Substance Registry System: (3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione(128366-05-2)
  • 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: 128366-05-2(Hazardous Substances Data)

128366-05-2 Usage

Uses

Used in Pharmaceutical Industry:
(3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione is used as a pharmaceutical candidate for its potential therapeutic effects. Its unique structure and functional groups may contribute to its pharmacological activity, making it a promising compound for further research and development in the field of medicine.
Used in Research and Development:
(3E)-3-[(butylamino)(hydroxy)methylidene]quinoline-2,4(1H,3H)-dione is used as a research compound for studying its pharmacological properties and potential applications. Scientists and researchers may investigate its interactions with biological targets, mechanisms of action, and efficacy in treating various diseases or conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 128366-05-2 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 128366-05:
(8*1)+(7*2)+(6*8)+(5*3)+(4*6)+(3*6)+(2*0)+(1*5)=132
132 % 10 = 2
So 128366-05-2 is a valid CAS Registry Number.

128366-05-2SDS

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 N-butyl-4-hydroxy-2-oxo-1H-quinoline-3-carboxamide

1.2 Other means of identification

Product number -
Other names N-Butyl-4-hydroxy-2-oxo-1,2-dihydro-3-quinolinecarboxamide

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:128366-05-2 SDS

128366-05-2Downstream Products

128366-05-2Relevant articles and documents

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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