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573674-19-8

1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester, also known as Shinorin, is a chemical compound with the molecular formula C18H14O3. It is a versatile organic compound that has been identified for its potential applications in various industries due to its unique properties.
Used in Pharmaceutical Industry:
1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester is used as an active pharmaceutical ingredient for its antioxidant and anti-inflammatory properties, which can contribute to the development of treatments for various diseases, including cancer and cardiovascular disorders.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester is utilized as a key component in the formulation of various agrochemical products, potentially enhancing crop protection and yield.
Used in Dye and Pigment Manufacturing:
1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester is used as a colorant in the production of dyes and pigments, offering a range of vibrant colors for use in various applications, such as textiles, plastics, and printing inks.
Used in Skincare and Cosmetic Products:
Due to its antioxidant and anti-inflammatory properties, 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester is used as an ingredient in skincare and cosmetic products to provide potential benefits to the skin, such as reducing inflammation and protecting against oxidative stress.

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  • 573674-19-8 Structure

  • Basic information

    1. Product Name: 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester
    2. Synonyms: 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester;4-hydroxyphenyl ester;WBJJAYLMKUGBCP-UHFFFAOYSA-N
    3. CAS NO:573674-19-8
    4. Molecular Formula: C17H12O3
    5. Molecular Weight: 264.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 573674-19-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 471.2°C at 760 mmHg
    3. Flash Point: 203.9°C
    4. Appearance: /
    5. Density: 1.286g/cm3
    6. Vapor Pressure: 1.68E-09mmHg at 25°C
    7. Refractive Index: 1.68
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester(573674-19-8)
    12. EPA Substance Registry System: 1-Naphthalenecarboxylic acid, 4-hydroxyphenyl ester(573674-19-8)

  • 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: 573674-19-8(Hazardous Substances Data)

573674-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 573674-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,3,6,7 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 573674-19:
(8*5)+(7*7)+(6*3)+(5*6)+(4*7)+(3*4)+(2*1)+(1*9)=188
188 % 10 = 8
So 573674-19-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H12O3/c18-13-8-10-14(11-9-13)20-17(19)16-7-3-5-12-4-1-2-6-15(12)16/h1-11,18H

573674-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-hydroxyphenyl) naphthalene-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Naphthalenecarboxylic acid,4-hydroxyphenyl 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:573674-19-8 SDS

573674-19-8Downstream Products

573674-19-8Relevant articles and documents

Guaiazulene-based phenolic radical scavengers: Synthesis, properties, and EPR studies of their reaction with oxygen-centred radicals

Franchi, Emanuela,Ingrosso, Giovanni,Marchetti, Fabio,Pinzino, Calogero

, p. 5003 - 5018 (2003)

A variety of phenolic derivatives 4, carrying the guaiazulene moiety, were prepared starting from guaiazulene. Compounds 4 react with oxygen-centred radicals exhibiting chromotropic behaviour. The radical scavenging power of these compounds was evaluated

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