Interesting facts
Interesting Facts about 1-(3-bromophenyl)ethanone
1-(3-bromophenyl)ethanone, also known as 3-bromoacetophenone, is a fascinating compound with unique properties and applications in the field of chemistry. Here are some notable aspects:
- Chemical Structure: This compound features a ketone functional group with a bromine atom substituent on the aromatic ring, contributing to its diverse reactivity. The presence of the bromine atom often enhances electrophilicity, making it a valuable building block in organic synthesis.
- Application in Organic Synthesis: 1-(3-bromophenyl)ethanone is frequently utilized as an intermediate in the synthesis of various organic compounds, especially in pharmaceutical research. Its ability to undergo substitution reactions opens avenues for creating complex molecular structures.
- Role in Material Science: The unique properties of this compound make it a candidate for studies in material science, particularly in creating novel polymers and dyes. Its aromatic nature contributes to stability and color retention.
- Biological Activity: Compounds containing similar structures have been investigated for their biological properties. Some derivatives exhibit antitumor, antimicrobial, and anti-inflammatory activities, indicating that 1-(3-bromophenyl)ethanone could be a starting point for new drug development.
- Environmental Considerations: As with many organic halides, the environmental impact of 1-(3-bromophenyl)ethanone must be assessed. Research into the biodegradability and toxicity of brominated compounds is crucial for assessing their environmental safety.
In conclusion, 1-(3-bromophenyl)ethanone represents an intriguing example of how a simple chemical structure can lead to a myriad of applications across various fields of chemistry. With ongoing research and development, its full potential continues to unfold!
Synonyms
3'-Bromoacetophenone
m-Bromoacetophenone
Ethanone, 1-(3-bromophenyl)-
3-BROMOACETOPHENONE
NSC 46620
DTXSID40870941
EINECS 218-396-0
DTXCID70818619
218-396-0
jyaqyxovohjrcs-uhfffaoysa-n
2142-63-4
1-(3-Bromophenyl)ethanone
1-(3-bromophenyl)ethan-1-one
Acetophenone, 3'-bromo-
MFCD00000083
1-(3-Bromo-phenyl)-ethanone
1-Acetyl-3-bromobenzene
NSC-46620
3 inverted exclamation mark -Bromoacetophenone
3-bromo acetophenone
NSC46620
3`-Bromoacetophenone
acetophenone, m-bromo-
(3-bromophenyl)ethanone
3a(2)-Bromoacetophenone
SCHEMBL3169
H4GKS4UK72
1-(3-bromophenyl)-ethanone
(3-bromophenyl)methyl ketone
3'-BROMOACETOPHENONE,
1-(3-Bromophenyl)ethanone #
CHEMBL5271897
STR01011
STL264115
AKOS000119026
CS-W009131
FB34687
PS-4704
SY001472
DB-028406
3'-Bromoacetophenone, ReagentPlus(R), 99%
B0536
NS00048618
EN300-19147
D70815
1-(3-Bromophenyl)ethanone; 1-Acetyl-3-bromobenzene
doi:10.14272/JYAQYXOVOHJRCS-UHFFFAOYSA-N.1
3'-Bromoacetophenone, Vetec(TM) reagent grade, 98%
Q63409213
F0001-0765
Z104472956
Solubility of 1-(3-bromophenyl)ethanone
1-(3-bromophenyl)ethanone, a compound with interesting structural features, demonstrates specific solubility characteristics that make it notable in various chemical contexts.
Solubility Behavior
To understand its solubility, one must consider several key factors:
In practice, it is often stated that “the solubility of a compound is a reflection of its molecular characteristics and interactions with solvents.” Therefore, one can predict:
Overall, the solubility profile of 1-(3-bromophenyl)ethanone not only aids in understanding its chemical behavior but also serves as a guide for its application in synthesis and reactions where solubility plays a pivotal role.