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Ethyl 2-methylquinoline-6-carboxylate is a chemical compound belonging to the class of organic compounds known as quinoline carboxylic acids. It features a quinoline ring system and a carboxylate group, with the systematic name of ethyl 2-methylquinoline-6-carboxylate. ethyl2-methylquinoline-6-carboxylate has a broad spectrum of potential applications across various fields, including pharmaceuticals, medicine, and chemical-based industries. Its appearance, stability, solubility, and other physicochemical properties are determined by its molecular structure and interactions with other substances.

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  • 855763-77-8 Structure
  • Basic information

    1. Product Name: ethyl2-methylquinoline-6-carboxylate
    2. Synonyms: ethyl2-methylquinoline-6-carboxylate;ethyl4-hydroxy-2-methylquinoline-6-carboxylate;2-Methylquinoline-6-carboxylic acid ethyl ester;2-Methyl-6-quinolinecarboxylic acid ethyl ester
    3. CAS NO:855763-77-8
    4. Molecular Formula: C13H13NO2
    5. Molecular Weight: 215.25
    6. EINECS: N/A
    7. Product Categories: Heterocyclic Compounds;Quinolines;quinoline
    8. Mol File: 855763-77-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 334.4 °C at 760 mmHg
    3. Flash Point: 156.1 °C
    4. Appearance: /Solid
    5. Density: 1.148 g/cm3
    6. Vapor Pressure: 0.000128mmHg at 25°C
    7. Refractive Index: 1.591
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 4.95±0.43(Predicted)
    11. CAS DataBase Reference: ethyl2-methylquinoline-6-carboxylate(CAS DataBase Reference)
    12. NIST Chemistry Reference: ethyl2-methylquinoline-6-carboxylate(855763-77-8)
    13. EPA Substance Registry System: ethyl2-methylquinoline-6-carboxylate(855763-77-8)
  • 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: 855763-77-8(Hazardous Substances Data)

855763-77-8 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 2-methylquinoline-6-carboxylate is used as an active pharmaceutical ingredient for the development of new drugs. Its unique molecular structure and properties make it a promising candidate for the treatment of various diseases and conditions.
Used in Medicinal Chemistry:
Ethyl 2-methylquinoline-6-carboxylate is utilized as a key intermediate in the synthesis of various medicinal compounds. Its presence in the molecular structure can enhance the biological activity and therapeutic potential of the resulting compounds.
Used in Chemical-based Industries:
Ethyl 2-methylquinoline-6-carboxylate is employed as a versatile building block in the synthesis of a wide range of chemical products. Its reactivity and compatibility with other chemical entities make it suitable for various industrial applications, such as the production of dyes, pigments, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 855763-77-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,7,6 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 855763-77:
(8*8)+(7*5)+(6*5)+(5*7)+(4*6)+(3*3)+(2*7)+(1*7)=218
218 % 10 = 8
So 855763-77-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c1-3-16-13(15)11-6-7-12-10(8-11)5-4-9(2)14-12/h4-8H,3H2,1-2H3

855763-77-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H63213)  Ethyl 2-methylquinoline-6-carboxylate, 97%   

  • 855763-77-8

  • 1g

  • 529.0CNY

  • Detail
  • Alfa Aesar

  • (H63213)  Ethyl 2-methylquinoline-6-carboxylate, 97%   

  • 855763-77-8

  • 5g

  • 1784.0CNY

  • Detail

855763-77-8SDS

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 Ethyl 2-methylquinoline-6-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 2-methylquinoline-6-carboxylate

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:855763-77-8 SDS

855763-77-8Downstream Products

855763-77-8Relevant articles and documents

Assembly of Diversely Substituted Quinolines via Aerobic Oxidative Aromatization from Simple Alcohols and Anilines

Li, Jixing,Zhang, Jinlong,Yang, Huameng,Jiang, Gaoxi

supporting information, p. 3284 - 3290 (2017/03/23)

An aerobic oxidative aromatization of simple aliphatic alcohols and anilines under the Pd(OAc)2/2,4,6-Collidine/Br?nsted acid catalytic system has been established, providing a direct approach for the preparation of diverse substituted quinoline derivatives in high yields with wide functional group tolerance. Practically, the protocol can be easily scaled up to gram-scale and was utilized in the concise formal synthesis of a promising herbicide candidate.

Preparation method of quinoline derivative

-

Paragraph 0101; 0102, (2017/06/02)

The invention provides a preparation method of a quinoline derivative. The method includes the steps of: in the presence of an oxidizing agent, adding a catalyst, then adding aniline or aromatic amine with different substituents, at the same time adding alcohol for reaction so as to prepare the quinoline derivative by one step. Specifically, the catalyst comprises a metal catalyst, an assistant catalyst I and an assistant catalyst II; the metal catalyst is a transition metal catalyst; the assistant catalyst I is an alkaline nitrogen-containing ligand; and the assistant catalyst II is an acidic compound. The quinoline derivative prepared by the method provided by the invention has stable performance and high purity. And the preparation method of the quinoline derivative can prepare quinoline, 2-methylquinoline, 8-hydroxyquinoline quinoline and other derivatives by one-step reaction, and the preparation method is simple and practicable. The preparation process does not produce new "three wastes", is environment-friendly, and provides a green and environment-friendly synthesis method. The preparation method has the characteristics of few raw material variety, little reaction equipment, few preparation step and low cost, and is more suitable for industrial production.

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