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2,4-Dibromo-5-hydroxybenzoic acid is a chemical compound characterized by the molecular formula C7H4Br2O4. It is a derivative of salicylic acid, featuring two bromine atoms and one hydroxyl group attached to a benzene ring. 2,4-Dibromo-5-hydroxybenzoic acid is known for its potential applications in the synthesis of pharmaceuticals, agricultural chemicals, and materials for electronic and optical devices, as well as for its possible anti-inflammatory and antioxidant properties.

14348-39-1

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14348-39-1 Usage

Uses

Used in Pharmaceutical Synthesis:
2,4-Dibromo-5-hydroxybenzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agricultural Chemicals:
In the agricultural industry, 2,4-Dibromo-5-hydroxybenzoic acid is utilized as a precursor for the production of agrochemicals, contributing to the development of more effective and environmentally friendly pesticides and herbicides.
Used in Electronic and Optical Materials:
2,4-Dibromo-5-hydroxybenzoic acid is employed as a building block in the creation of new materials for electronic and optical devices. Its chemical properties make it suitable for use in the development of advanced materials with improved performance characteristics.
Used in Anti-inflammatory and Antioxidant Research:
Due to its potential anti-inflammatory and antioxidant properties, 2,4-Dibromo-5-hydroxybenzoic acid is used in scientific research to explore its therapeutic potential in treating inflammation-related conditions and oxidative stress disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 14348-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14348-39:
(7*1)+(6*4)+(5*3)+(4*4)+(3*8)+(2*3)+(1*9)=101
101 % 10 = 1
So 14348-39-1 is a valid CAS Registry Number.

14348-39-1SDS

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 2,4-Dibromo-5-hydroxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2,4-dibromo-5-hydroxy-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:14348-39-1 SDS

14348-39-1Relevant academic research and scientific papers

Method for photocatalytic synthesis of polybrominated phenol compound in water phase

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Paragraph 0012; 0031, (2019/08/30)

The invention discloses a method for photocatalytic synthesis of a polybrominated phenol compound in a water phase, comprising the following steps: adding a catalytic amount of a radical initiator, aphenol derivative and low-toxic and cheap bromide salt and water into a reaction vessel, reacting at room temperature at 5 W power in a photocatalytic reactor for a certain period, extracting with ethyl acetate and then re-crystallizing to obtain a polybrominated phenol compound. The above radical initiator is eosin, azobisisobutanol, sodium persulfate, ammonium persulfate or potassium persulfate.The free radical initiator and the bromine salt are cheap and easily available, and the method is an ideal synthesis method of the polybrominated phenol compound. According to the method, low-toxicity bromine salt instead of liquid bromine is used to carry out a bromination reaction, unstable and explosive hydrogen peroxide is replaced with the cheap and easily-available free radical initiator, and an emerging photocatalytic method is used. The polybrominated phenol compound can be obtained in a high yield by only using a 5W power lamp for the reaction, the reaction selectivity is high, by-products are less, and the post-treatment is simple.

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