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CAS

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487-71-8

2-Methoxy-benzene-1,3,5-triol, also known as gentisic acid, is a phenolic compound found in plants such as gentian root and fruits like strawberries. It possesses antioxidant properties, which help protect cells and tissues from damage caused by free radicals. Additionally, it has been studied for its potential anti-inflammatory and anti-cancer properties.
Used in Pharmaceutical Industry:
2-Methoxy-benzene-1,3,5-triol is used as a pharmaceutical ingredient for its antioxidant, anti-inflammatory, and anti-cancer properties. It can be incorporated into medications to help protect cells and tissues from damage and potentially treat inflammatory and cancerous conditions.
Used in Food Industry:
2-Methoxy-benzene-1,3,5-triol is used as a flavoring agent in the food industry. Its natural presence in fruits like strawberries makes it a suitable candidate for enhancing the flavor of various food products.
Used in Skincare Products:
2-Methoxy-benzene-1,3,5-triol is used as an ingredient in skincare products due to its antioxidant and anti-inflammatory properties. It can help protect the skin from damage caused by free radicals and potentially reduce inflammation and signs of aging.

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  • 487-71-8 Structure

  • Basic information

    1. Product Name: 2-METHOXY-BENZENE-1,3,5-TRIOL
    2. Synonyms: 2-METHOXY-PHLOROGLUCINOL;2-METHOXY-BENZENE-1,3,5-TRIOL;2,4,6-Trihydroxy-1-methoxybenzene;2-Methoxy-1,3,5-benzenetriol;Iretol
    3. CAS NO:487-71-8
    4. Molecular Formula: C7H8O4
    5. Molecular Weight: 156.14
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 487-71-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 323.1°Cat760mmHg
    3. Flash Point: 149.2°C
    4. Appearance: /
    5. Density: 1.436g/cm3
    6. Vapor Pressure: 0.000141mmHg at 25°C
    7. Refractive Index: 1.627
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-METHOXY-BENZENE-1,3,5-TRIOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-METHOXY-BENZENE-1,3,5-TRIOL(487-71-8)
    12. EPA Substance Registry System: 2-METHOXY-BENZENE-1,3,5-TRIOL(487-71-8)

  • 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: 487-71-8(Hazardous Substances Data)

487-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 487-71-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 487-71:
(5*4)+(4*8)+(3*7)+(2*7)+(1*1)=88
88 % 10 = 8
So 487-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O4/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3,8-10H,1H3

487-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxybenzene-1,3,5-triol

1.2 Other means of identification

Product number -
Other names 2,4,6-trihydroxyanisole

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:487-71-8 SDS

487-71-8Relevant articles and documents

Total Synthesis of Hispidulin and the Structural Basis for Its Inhibition of Proto-oncogene Kinase Pim-1

Chao, Shi-Wei,Su, Ming-Yuan,Chiou, Lih-Chu,Chen, Liang-Chieh,Chang, Chung-I,Huang, Wei-Jan

, p. 1969 - 1976 (2015/09/08)

(Figure Presented). A new method is applied to synthesize hispidulin, a natural flavone with a broad spectrum of biological activities. Hispidulin exhibits inhibitory activity against the oncogenic protein kinase Pim-1. Crystallographic analysis of Pim-1 bound to hispidulin reveals a binding mode distinct from that of quercetin, suggesting that the binding potency of flavonoids is determined by their hydrogen-bonding interactions with the hinge region of the kinase. Overall, this work may facilitate construction of a library of hispidulin-derived compounds for investigating the structure-activity relationship of flavone-based Pim-1 inhibitors.

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

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