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Ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate is a complex organic compound belonging to the quinoline family. It is characterized by its heterocyclic structure, which includes a nitrogen atom in the ring, and features a chlorine atom, a cyclopropyl group, and a methyl group as substituents. ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate is known for its potential applications in the pharmaceutical industry due to its unique chemical properties.

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  • High purity 7-Chloro-1-cyclopropyl-8-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid ethyl ester CAS No.:103877-51-6

    Cas No: 103877-51-6

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  • 103877-51-6 Structure
  • Basic information

    1. Product Name: ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate
    2. Synonyms: 7-Chloro-1-cyclopropyl-8-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid ethyl ester
    3. CAS NO:103877-51-6
    4. Molecular Formula: C16H16ClNO3
    5. Molecular Weight: 305.76
    6. EINECS: 600-496-4
    7. Product Categories: N/A
    8. Mol File: 103877-51-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 448.7°C at 760 mmHg
    3. Flash Point: 225.2°C
    4. Appearance: N/A
    5. Density: 1.362g/cm3
    6. Vapor Pressure: 3.04E-08mmHg at 25°C
    7. Refractive Index: 1.62
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: -3.24±0.40(Predicted)
    11. CAS DataBase Reference: ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate(CAS DataBase Reference)
    12. NIST Chemistry Reference: ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate(103877-51-6)
    13. EPA Substance Registry System: ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate(103877-51-6)
  • 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: 103877-51-6(Hazardous Substances Data)

103877-51-6 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure allows it to serve as a building block in the development of new medications, particularly those targeting specific biological pathways or receptors.
As a pharmaceutical intermediate, ethyl 7-chloro-1-cyclopropyl-8-methyl-4-oxo-quinoline-3-carboxylate is utilized for the following reasons:
1. Its heterocyclic structure can be modified to create a variety of drug candidates with different biological activities.
2. The presence of functional groups, such as the chlorine atom and the cyclopropyl group, enables further chemical reactions to produce more complex molecules with specific therapeutic properties.
3. The compound's structural diversity makes it a valuable asset in the design and synthesis of novel drugs, potentially leading to the discovery of new treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 103877-51-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,7 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103877-51:
(8*1)+(7*0)+(6*3)+(5*8)+(4*7)+(3*7)+(2*5)+(1*1)=126
126 % 10 = 6
So 103877-51-6 is a valid CAS Registry Number.

103877-51-6Relevant articles and documents

CRYSTALLINE FORM OF OZENOXACIN AND PROCESSES FOR PREPARATION THEREOF

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, (2020/05/12)

The present invention relates to a crystalline form of 1-cyclopropyl-8-methyl-7- (5-methyl-6-(methylamino)pyridin-3-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid the compound of formula-1, which is represented by the following structural formula-1. The

Preparation method of Ozenoxacin and intermediates thereof

-

, (2019/01/05)

The invention provides compounds represented by the formula (IIIb) and a preparation method thereof. The invention also provides an application of the compound represented by the formula (IIIb) as a key intermediate in Ozenoxacin preparation.

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