Interesting facts
Interesting Facts About 1-(3-Nitrophenyl)ethanone
1-(3-Nitrophenyl)ethanone, a member of the ketone family, presents a fascinating structure and significant applications in various fields of science. Here are some key points that highlight its importance:
- Chemical Structure: The compound consists of a phenyl ring substituted with a nitro group and attached to an ethanone moiety. This arrangement contributes to its unique chemical properties.
- Synthetic Applications: It serves as a crucial intermediate in the synthesis of various pharmaceutical compounds. Many drugs harness its reactivity to develop more complex molecules.
- Biological Activity: The nitro group in the compound is known to impart potential biological properties, making it interesting for research in medicinal chemistry. It has shown promise in anti-inflammatory and antibacterial activities.
- Electrophilic Character: The presence of both the ketone and nitro functionalities indicates its potential as an electrophile, making it a candidate for nucleophilic substitution reactions.
- Research Significance: Ongoing studies are investigating the environmental impacts of 1-(3-nitrophenyl)ethanone and its derivatives, particularly in relation to sustainability and green chemistry.
To quote a prominent chemist, "Understanding the behavior of such compounds leads us closer to innovations in drug design and environmental sciences."
Thus, 1-(3-nitrophenyl)ethanone is a compound that stands at the intersection of organic chemistry and biochemistry, showcasing the ever-evolving landscape of chemical research.
Synonyms
3'-Nitroacetophenone
121-89-1
3-Nitroacetophenone
M-NITROACETOPHENONE
1-(3-Nitrophenyl)ethanone
Ethanone, 1-(3-nitrophenyl)-
m-Acetylnitrobenzene
Acetophenone, 3'-nitro-
Methyl 3-nitrophenyl ketone
USAF MA-1
3-Nitroacetofenon
(3-Nitrophenyl) methyl ketone
NSC 5511
3-Nitroacetofenon [Czech]
3-nitro acetophenone
MFCD00007259
CCRIS 2330
1-(3-nitrophenyl)ethan-1-one
HSDB 2710
1-Acetyl-3-nitrobenzene
EINECS 204-504-3
1-(3-nitrophenyl)-ethanone
SU4B5T763F
DTXSID1025722
AI3-02242
NSC-5511
DTXCID305722
M-NITROACETOPHENONE [HSDB]
3'-NITROACETOPHENONE;3'-Nitroacetophenone
1-{3-nitrophenyl}ethanone
UNII-SU4B5T763F
3Nitroacetofenon
3Nitroacetophenone
mAcetylnitrobenzene
3'Nitroacetophenone
3-acetylnitrobenzene
3'-Nitro-acetophenone
Acetophenone, 3'nitro
acetophenone, m-nitro-
1(3Nitrophenyl)ethanone
Methyl 3nitrophenyl ketone
3 inverted exclamation mark -Nitroacetophenone
WLN: WNR CV1
(3-nitrophenyl)methylketone
Cambridge id 5102515
Ethanone, 1(3nitrophenyl)
SCHEMBL54610
(3Nitrophenyl) methyl ketone
MLS002415744
1-(3-Nitrophenyl)ethanone #
SCHEMBL2617114
CHEMBL1327526
NSC5511
HMS3039O12
STR00971
Tox21_200737
STL183285
AKOS000119652
AKOS040761108
CS-W020548
FN01003
NCGC00091314-01
NCGC00091314-02
NCGC00258291-01
AC-25903
CAS-121-89-1
SMR001370908
SY001185
DB-041636
3'-Nitroacetophenone, ReagentPlus(R), 99%
N0109
NS00020942
3 inverted exclamation marka-Nitroacetophenone
EN300-18002
3'-Nitroacetophenone, purum, >=98.0% (GC)
D70891
AQ-917/40187877
3'-Nitroacetophenone, Vetec(TM) reagent grade, 98%
Q27289401
Z57127467
F3098-5170
m-Nitroacetophenone; 1-(3-Nitrophenyl)ethanone;3-Nitroacetophenone
204-504-3
Solubility of 1-(3-nitrophenyl)ethanone
1-(3-nitrophenyl)ethanone, which has the chemical formula C9H9NO3, exhibits intriguing solubility characteristics that are noteworthy for various applications and studies. The solubility of this compound can be attributed to its molecular structure and the presence of functional groups that influence interactions with solvents.
Key points regarding the solubility of 1-(3-nitrophenyl)ethanone include:
Overall, understanding the solubility behavior of 1-(3-nitrophenyl)ethanone is essential for its effective use in chemical reactions and applications. As one researcher noted, "solubility serves as a gateway to exploring the versatility and reactivity of chemical compounds." Therefore, detailed studies on solubility behaviors can unveil profound insights into not only 1-(3-nitrophenyl)ethanone but also similar compounds in its class.