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4-Bromo-3,5-dichlorobenzoic acid is a complex organic compound with a benzene ring as its core structure, featuring one bromine (Br), two chlorine (Cl) atoms, and a carboxyl group (-COOH) attached to it. This aromatic compound is a type of halogenated benzoic acid, known for its potential applications in organic synthesis, biochemical research, and pharmaceutical development. Due to its halogenated nature, it requires careful handling and storage to ensure safety.

117738-75-7

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117738-75-7 Usage

Uses

Used in Organic Synthesis:
4-Bromo-3,5-dichlorobenzoic acid is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable building block for the creation of new molecules with specific properties.
Used in Biochemical Research:
In biochemical research, 4-Bromo-3,5-dichlorobenzoic acid serves as a valuable tool for studying enzyme activity, protein interactions, and other biological processes. Its halogenated structure can be used to probe the binding sites of enzymes and other biomolecules, providing insights into their mechanisms of action.
Used in Pharmaceutical Development:
4-Bromo-3,5-dichlorobenzoic acid is utilized in the development of pharmaceuticals, particularly as a precursor for the synthesis of drug candidates. Its unique chemical properties can be leveraged to design and optimize the structure of new drugs, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Synthesis Industry:
4-Bromo-3,5-dichlorobenzoic acid is used as a starting material or intermediate in the chemical synthesis industry for the production of various specialty chemicals, dyes, and pigments. Its reactivity and functional groups make it suitable for a wide range of chemical transformations.
Used in Environmental Analysis:
In environmental analysis, 4-Bromo-3,5-dichlorobenzoic acid can be employed as a reference compound or standard for the development and validation of analytical methods. Its distinct chemical properties can be used to evaluate the performance of chromatographic, spectroscopic, and other analytical techniques.
Used in Material Science:
4-Bromo-3,5-dichlorobenzoic acid can be utilized in material science for the development of new materials with specific properties, such as polymers, coatings, and adhesives. Its halogenated structure can contribute to the desired characteristics of these materials, such as thermal stability, chemical resistance, and adhesion properties.

Check Digit Verification of cas no

The CAS Registry Mumber 117738-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,3 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 117738-75:
(8*1)+(7*1)+(6*7)+(5*7)+(4*3)+(3*8)+(2*7)+(1*5)=147
147 % 10 = 7
So 117738-75-7 is a valid CAS Registry Number.

117738-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-3,5-dichlorobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Brom-3,5-dichlor-benzoesaeure

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:117738-75-7 SDS

117738-75-7Relevant academic research and scientific papers

3,5-dichloro-4-bromoisoquinoline derivative, and preparation method and application thereof

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, (2019/10/04)

The invention specifically relates to a novel compound, i.e., a 3,5-dichloro-4-bromoisoquinoline derivative, and a preparation method and application thereof, belonging to the technical field of pharmaceutical synthesis. 3,5-dichloro-4-bromoisoquinoline and the derivative thereof are obtained by ring closure of 3,5-dichloro-4-bromobenzene haloethylamine through a Friedel-Crafts alkylation reaction. The 3,5-dichloro-4-bromoisoquinoline and the derivative can be used for synthesizing the important intermediate 3,5-dichloro-4-carboxylisoquinoline of Lifitegrast. According to a technical scheme in the invention, low-cost and well-supplied 2,6-dichloroaniline is used as a starting material; and the preparation method comprises a plurality steps of reactions with mild conditions, mature operation and yield of 85% or more, and each step of reaction has passed pilot-scale test, so the feasibility of industrial conversion of the method is very high and overall production cost can be greatly reduced.

Pesticidal compounds

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, (2008/06/13)

Bicyclooctane pesticides of the formula are prepared by cyclisation of In these formulae R may be various organic groups and is preferably n-butyl or n-propyl while R2 is a polysubstituted phenyl group.

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