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2,6-dichloro-4-hydroxy-3,5-dimethoxybenzoic acid, commonly known as rosmarinic acid, is a naturally occurring phenolic compound found in a variety of plants such as rosemary, oregano, and lemon balm. It exhibits a range of beneficial properties, including antioxidant, anti-inflammatory, antimicrobial, and anti-cancer activities. Rosmarinic acid has been the focus of research for its potential therapeutic effects on various conditions and its use in traditional medicine for cognitive enhancement.

20624-96-8

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20624-96-8 Usage

Uses

Used in Pharmaceutical Applications:
Rosmarinic acid is utilized as a therapeutic agent for its potential to alleviate allergies, asthma, and inflammatory diseases. Its anti-inflammatory properties make it a promising candidate for treating these conditions.
Used in Traditional Medicine:
In traditional medicine, rosmarinic acid is used as a cognitive enhancer to improve memory and cognitive function, potentially benefiting individuals with cognitive decline or memory-related disorders.
Used in Skincare Products:
Rosmarinic acid is employed in skincare formulations as an ingredient to protect the skin from harmful UV radiation and oxidative stress. Its antioxidant properties contribute to skin health and may help prevent premature aging and other skin conditions.
Used in Antioxidant Formulations:
Due to its potent antioxidant capabilities, rosmarinic acid is used in various antioxidant formulations to combat oxidative stress and support overall health.
Used in Antimicrobial Applications:
Rosmarinic acid's antimicrobial properties make it suitable for use in antimicrobial applications, potentially serving as a natural alternative to synthetic antimicrobial agents in certain products.
Used in Anti-cancer Research:
Rosmarinic acid is extensively studied for its anti-cancer properties, with ongoing research exploring its potential to inhibit cancer cell growth and its use in combination with conventional cancer therapies to enhance treatment efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 20624-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,2 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20624-96:
(7*2)+(6*0)+(5*6)+(4*2)+(3*4)+(2*9)+(1*6)=88
88 % 10 = 8
So 20624-96-8 is a valid CAS Registry Number.

20624-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-4-hydroxy-3,5-dimethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2,6-dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid

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:20624-96-8 SDS

20624-96-8Downstream Products

20624-96-8Relevant academic research and scientific papers

Preparation and properties of chlorinated syringic acids, acetosyringones, acetoguaiacones and methoxy-p-hydroquinones components of pulp bleaching effluents

Smith,Wearne,Wallis

, p. 69 - 80 (2007/10/03)

A range of chlorinated phenols which serve as standards for compounds occurring in effluents from the bleaching of wood pulps with chlorine-containing reagents has been prepared. The chlorinated phenols include chlorosyringic acids, chloroacetosyringones, chloroacetoguaiacones, 5-chloro-2-methoxy-p-hydroquinone and chloro-2,6-dimethoxy-p-hydroquinones. With the exception of the ring-chlorinated acetoguaiacones which were prepared by reaction of chlorovanillin acetates with diazomethane, the compounds were obtained by direct chlorination of appropriate phenols or their acetates. Gas chromatographic and mass spectrometric data for the acetylated phenols are given.

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