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Methyl 6-hydroxyquinoline-2-carboxylate is a chemical compound with the molecular formula C12H9NO3, belonging to the quinoline family. It features a hydroxyl group and a carboxylic ester functional group, which contribute to its diverse applications in various industries.

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  • 429687-75-2 Structure
  • Basic information

    1. Product Name: Methyl 6-hydroxyquinoline-2-carboxylate
    2. Synonyms: 2-Quinolinecarboxylic acid, 6-hydroxy-, methyl ester
    3. CAS NO:429687-75-2
    4. Molecular Formula: C11H9NO3
    5. Molecular Weight: 203.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 429687-75-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 6-hydroxyquinoline-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 6-hydroxyquinoline-2-carboxylate(429687-75-2)
    11. EPA Substance Registry System: Methyl 6-hydroxyquinoline-2-carboxylate(429687-75-2)
  • 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: 429687-75-2(Hazardous Substances Data)

429687-75-2 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Methyl 6-hydroxyquinoline-2-carboxylate serves as a building block in the synthesis of pharmaceuticals and agrochemicals. Its antibacterial, antifungal, and antiviral properties make it a promising candidate for the development of new drugs.
Used in Chelating Applications:
As a chelating agent, Methyl 6-hydroxyquinoline-2-carboxylate forms complexes with metal ions. This property has been investigated for its potential application in corrosion inhibition, offering a solution for protecting metal surfaces from degradation.
Used in Dye and Pigment Manufacturing:
Methyl 6-hydroxyquinoline-2-carboxylate is utilized in the manufacturing of dyes and pigments due to its ability to produce a range of colors. Its chemical structure allows for the creation of various organic compounds with different color properties, making it valuable in this industry.

Check Digit Verification of cas no

The CAS Registry Mumber 429687-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,9,6,8 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 429687-75:
(8*4)+(7*2)+(6*9)+(5*6)+(4*8)+(3*7)+(2*7)+(1*5)=202
202 % 10 = 2
So 429687-75-2 is a valid CAS Registry Number.

429687-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-hydroxyquinoline-2-carboxylate

1.2 Other means of identification

Product number -
Other names 6-HYDROXY-2-QUINOLINECARBOXYLIC ACID METHYL ESTER

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:429687-75-2 SDS

429687-75-2Relevant articles and documents

Thio hydantoin ternary and circular androgen receptor antagonists and use thereof (by machine translation)

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Paragraph 0193; 0220; 0221, (2017/08/02)

The invention relates to the field of pharmaceutical chemistry, and in particular relates to a category of thio hydantoin and indoline skeleton has the role of the anti-prostate cancer compound (I) and (II), a method for preparing these compounds, these c

6-HETEROARYLOXY- OR 6-ARYLOXY-QUINOLINE-2-CARBOXAMIDES AND METHOD OF USE

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, (2015/09/22)

Compounds of formula (I) and pharmaceutically acceptable salts, esters, amides, or radiolabelled forms thereof, wherein R1, R2, and R3 are as defined in the specification, are useful in treating conditions or disorders prevented by or ameliorated by voltage-gated sodium channels, e.g., Nav1.7 and/or Nav1.8. Methods for making the compounds are disclosed. Also disclosed are pharmaceutical compositions of compounds of formula (I), and methods for using such compounds and compositions.

Bicyclo 4.4.0 antiviral derivatives

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Page/Page column 32, (2008/06/13)

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with amido piperazine derivatives. These compounds possess unique antiviral activity

Heterocycle annulation of enolizable vinyl quinone imides. Dihydroquinolines and quinolines from thermal 6π-electrocyclizations and indoles from photochemical cyclizations

Parker, Kathlyn A.,Mindt, Thomas L.

, p. 4265 - 4268 (2007/10/03)

(equation presented) Enolizable vinyl quinone mono-and diimide substrates yield protected 6-hydroxy and 6-amino dihydroquinolines by thermal electrocyclization. Aromatization provides the corresponding quinolines in quantitative yields. The quinone monoimide substrates undergo clean photochemical conversion to 5-hydroxy indoles.

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