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4-Hydroxy-naphtalene-1-carboxylic acid methyl ester, with the molecular formula C13H10O3, is a white solid chemical compound known for its melting point of 163-165°C and solubility in organic solvents. It is a versatile intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals, and is also used in the production of dyes, pigments, and optical brighteners. Due to its potential hazards, it requires careful handling and storage.

13041-63-9

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13041-63-9 Usage

Uses

Used in Organic Synthesis:
4-Hydroxy-naphtalene-1-carboxylic acid methyl ester is used as an intermediate in organic synthesis for the production of a wide range of compounds, including pharmaceuticals and agrochemicals. Its unique chemical structure allows for various chemical reactions, making it a valuable component in the synthesis process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Hydroxy-naphtalene-1-carboxylic acid methyl ester is used as a key intermediate in the synthesis of various drugs. Its presence in the molecular structure of these drugs contributes to their therapeutic properties and effectiveness in treating different medical conditions.
Used in Agrochemical Industry:
4-Hydroxy-naphtalene-1-carboxylic acid methyl ester is also utilized in the agrochemical industry as an intermediate in the production of various agrochemicals. Its role in the synthesis of these compounds helps to enhance their effectiveness in protecting crops and improving agricultural productivity.
Used in Dye and Pigment Manufacturing:
In the dye and pigment manufacturing industry, 4-Hydroxy-naphtalene-1-carboxylic acid methyl ester is used as a raw material for the production of dyes, pigments, and optical brighteners. Its chemical properties contribute to the color intensity and stability of these products, making them suitable for various applications in textiles, plastics, and other industries.
Used in Optical Brightener Production:
4-Hydroxy-naphtalene-1-carboxylic acid methyl ester is used as a key component in the production of optical brighteners. These brighteners are used to enhance the appearance of various materials by reflecting light more effectively, providing a brighter and more vivid appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 13041-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13041-63:
(7*1)+(6*3)+(5*0)+(4*4)+(3*1)+(2*6)+(1*3)=59
59 % 10 = 9
So 13041-63-9 is a valid CAS Registry Number.

13041-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-hydroxynaphthalene-1-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-naphthalin-1-carbonsaeuremethylester

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:13041-63-9 SDS

13041-63-9Downstream Products

13041-63-9Relevant academic research and scientific papers

Isomerization of 7-oxabenzonorbornadienes into naphthols catalyzed by [RuCl2(CO)3]2

Ballantine, Melissa,Menard, Michelle L.,Tam, William

supporting information; experimental part, p. 7570 - 7573 (2009/12/28)

(Chemical Equation Presented) Ruthenium-catalyzed isomerization of 7-oxanorbornadienes into naphthols was investigated. Among the various ruthenium catalysts tested, [RuCl2(CO)3]2 gave the highest yields in the isomerizati

Alkynyl halides in ruthenium(II)-catalyzed [2+2] cycloadditions of bicyclic alkenes

Allen, Anna,Villeneuve, Karine,Cockburn, Neil,Fatila, Elisabeth,Riddell, Nicole,Tam, William

experimental part, p. 4178 - 4192 (2009/05/27)

Ru-catalyzed [2+2] cycloadditions between bicyclic alkenes and alkynyl halides were found to occur in moderate to good yields. The presence of the halide moiety greatly enhances the reactivity of the alkyne component in the cycloaddition and can be transformed into a variety of products that are difficult or impossible to obtain by direct cycloaddition. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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