334792-76-6

Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-2-fluorobenzoic acid ethyl ester is used as an intermediate in the synthesis of pharmaceuticals for its unique chemical properties, enabling the development of new drugs with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, 3-bromo-2-fluorobenzoic acid ethyl ester is used as a building block for the production of various agrochemicals, contributing to the development of effective crop protection agents and other agricultural products.
Used in Organic Synthesis:
3-Bromo-2-fluorobenzoic acid ethyl ester is used as a reagent in organic synthesis processes, allowing for the creation of a wide range of chemical compounds with diverse applications across various industries.

InChI:InChI=1/C9H8BrFO2/c1-2-13-9(12)6-4-3-5-7(10)8(6)11/h3-5H,2H2,1H3

Upstream product

• 64-17-5 ethanol 
• 161957-56-8 3-bromo-2-fluorobenzoic acid 
• 1072-85-1 o-fluorobromobenzene 

Downstream Products

• 334792-77-7 ethyl 2-fluoro-3-(4-hydroxypiperidin-1-yl)benzoate 
• 871224-16-7 3-vinyl-2-fluorobenzoic acid ethyl ester 
• 1782070-22-7 3-((6-chloro-2-cyclopropyl-1-(1-ethyl-1H-pyrazol-4-yl)-7-fluoro-1H-indol-3-yl)thio)-2-fluorobenzoic acid 

Relevant academic research and scientific papers

AUTOTAXIN INHIBITORS AND USES THEREOF

Described herein are methods and compositions for the treatment of conditions, diseases, or disorders associated with autotaxin activity. The methods and compositions disclosed herein include the use of at least one autotaxin inhibitor compound.

AUTOTAXIN INHIBITOR COMPOUNDS

Described herein are compounds that are autotaxin inhibitors, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders associated with autotaxin activity.

AUTOTAXIN INHIBITOR COMPOUNDS

Described herein are compounds that are autotaxin inhibitors, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorde

Methods for the treatment of metabolic disorders by a selective small molecule autotaxin inhibitor

Described herein are methods and compositions for treatment or prevention of metabolic disorder(s) in an individual. The methods and compositions disclosed herein include the use of at least one autotaxin inhibitor compound.

COMPOUND HAVING 6-MEMBERED AROMATIC RING

An object of the present invention is to provide an agent for preventing or treating schizophrenia or the like, wherein the compound of the present invention has GPR52 agonist activity. [Means] A compound represented by the following formula (I) or salt t

Tricyclic pharmacophore-based molecules as novel integrin αvβ3 antagonists. Part IV: Preliminary control of αvβ3 selectivity by meta-oriented substitution

To establish the in vivo efficacy of αvβ3/αIIbβ3 dual antagonists possessing a tricyclic pharmacophore, a corresponding αvβ3-selective antagonist was required as a control. We initially too

m-SUBSTITUTED BENZOIC ACID DERIVATIVES EXHIBITING INTEGRIN ALPHA-V BETA-3 ANTAGONISM

An object of the present invention is to provide m-substituted benzoic acid derivatives having integrin αvβ3 antagonistic activity. The derivatives according to the present invention are compounds represented by formula (I) or pharmaceutically acceptable salts or solvates thereof, which are useful for the treatment or prevention of cardiovascular diseases, angiogenesis-related diseases, cerebrovascular diseases, cancers and metastasis thereof, immunological diseases, osteopathy and other diseases: wherein A represents an optionally substituted heterocyclic group containing two nitrogen atoms, a bicylic group or the like; D represents a bond, >NR4, >CR5R6, O, S, or -NR4-CR5R6-; X represents CH or N; R7 and R8 represent hydroxyl, alkyl or the like; Q represents >C=O or the like; R9 represents hydrogen, alkyl or the like; J represents a bond or alkylene; R10 represents optionally substituted hydroxyl, amino or the like; R11 represents hydrogen, alkyl or the like; m is 0 to 5; n is 0 to 4; and p and q are each 0 to 3.