4-Bromo-2,6-difluorobenzoic acid Chemical Properties

Melting point:

201-203°C

Boiling point:

271.7±40.0 °C(Predicted)

Density 

1.872±0.06 g/cm3(Predicted)

vapor pressure 

0-1.1Pa at 25-78℃

storage temp. 

Sealed in dry,Room Temperature

solubility 

soluble in Methanol

form 

powder to crystal

pka

2.11±0.10(Predicted)

color 

White to Light yellow to Light orange

InChIKey

IRHPJGPQWZEZRX-UHFFFAOYSA-N

LogP

2.5 at 25℃

CAS DataBase Reference

183065-68-1(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xi,Xn

Risk Statements 

22-36/37/38

Safety Statements 

26-37

WGK Germany 

3

HazardClass 

IRRITANT

HS Code 

29163100

4-Bromo-2,6-difluorobenzoic acid Usage And Synthesis

Description

4-Bromo-2,6-difluorobenzoic acid (4-Br-2,6-DFA) is an organic compound that holds significant prominence in scientific research. It serves as a crucial intermediate in the synthesis of various organic compounds and finds frequent utilization in laboratory experiments.

Chemical Properties

Off-white Cryst

Uses

In the realm of scientific research, 4-Bromo-2,6-difluorobenzoic acid enjoys wide-ranging usage. It serves as a pivotal intermediate in synthesizing an array of organic compounds. Moreover, its application extends to the synthesis of compounds such as insecticides and herbicides. Additionally, 4-Bromo-2,6-difluorobenzoic acid plays a crucial role in studying enzyme kinetics and has been instrumental in synthesizing diverse peptides and proteins. Although the complete mechanism of action of 4-Bromo-2,6-difluorobenzoic acid remains elusive, it is believed to function as a competitive inhibitor of enzymes like cytochrome P450, along with other enzymes involved in the metabolism of organic compounds.

Application

4-Bromo-2,6-difluorobenzoic acid is recognized as an inhibitor of acetylcholinesterase, an enzyme responsible for acetylcholine breakdown—a neurotransmitter vital for various physiological processes. In summary, 4-Bromo-2,6-difluorobenzoic acid (4-Br-2,6-DFA) is a highly valued organic compound within scientific research. Its extensive applications encompass serving as an intermediate in synthesizing diverse organic compounds, aiding in enzyme kinetics studies, and contributing to the synthesis of peptides and proteins. The precise mechanisms through which it operates are not fully understood, but it is recognized as a competitive inhibitor of certain enzymes.

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