Interesting facts
Interesting Facts about 1-Bromo-4-nitro-benzene
1-Bromo-4-nitro-benzene is a fascinating compound that presents a unique combination of properties due to the presence of both bromine and nitro groups attached to the benzene ring. Here are some notable aspects of this compound:
- Applications in Synthesis: This compound is often utilized in organic synthesis, particularly in the preparation of various pharmaceutical intermediates and agrochemicals. Its structure facilitates electrophilic aromatic substitution reactions.
- Reactivity: The nitro group at the para position acts as a strong electron-withdrawing group, which significantly influences the chemical reactivity of the benzene ring. This makes 1-bromo-4-nitro-benzene a valuable precursor in creating further functionalized compounds.
- Environmental Considerations: Like many bromo compounds, 1-bromo-4-nitro-benzene is subject to regulations due to its potential environmental impact. Understanding its chemical behavior in ecosystems is crucial for ensuring safety in applications.
- Safety Profile: Handling this compound requires caution. It can be hazardous, and proper safety measures should be taken to mitigate any health risks associated with exposure.
- Historical Context: Compounds similar to 1-bromo-4-nitro-benzene have been studied extensively since the development of synthetic organic chemistry in the early 20th century. Their utility in diverse fields highlights the progress made in chemical research.
Overall, 1-bromo-4-nitro-benzene serves as an excellent example of how modifications to a simple aromatic system can produce a compound with diverse applications and significant importance in the realm of organic chemistry.
Synonyms
1-Bromo-4-nitrobenzene
586-78-7
Benzene, 1-bromo-4-nitro-
CCRIS 3115
AI3-15384
NSC 3526
EINECS 209-583-8
DTXSID7060415
pBromonitrobenzene
pNitrobromobenzene
4bromonitrobenzene
4Nitrobromobenzene
pNitrophenyl bromide
4Nitrophenyl bromide
Benzene, 1bromo4nitro
DTXCID6042442
209-583-8
inchi=1/c6h4brno2/c7-5-1-3-6(4-2-5)8(9)10/h1-4
4-Bromonitrobenzene
P-BROMONITROBENZENE
4-Nitrobromobenzene
p-Nitrobromobenzene
4-bromo-1-nitrobenzene
1-bromo-4-nitro-benzene
MFCD00007280
4-Nitro-bromobenzene
NSC-3526
4-Nitrophenyl bromide
p-Nitrophenyl bromide
p-nitrophenylbromide
p-bromo nitrobenzene
p-nitro-bromobenzene
4-bromo nitrobenzene
4-bromo-nitrobenzene
4-bromonitro benzene
para-bromonitrobenzene
para-nitrobromobenzene
1-bromo4-nitrobenzene
4-(nitro)bromobenzene
4-nitrobenzene bromide
2-bromo-5-nitrobenzene
4-(nitro)-bromobenzene
1-Bromo 4-nitrobenzene
4-(nitro) -bromobenzene
1-bromanyl-4-nitro-benzene
SCHEMBL85535
ghl.PD_Mitscher_leg0.924
W2D6WLV889
1-Bromo-4-nitrobenzene, 99%
NSC3526
STR03424
p-Nitrobromobenzene, liquid or solid
STK291012
AKOS000119958
FB139867
DB-019086
B0624
CS-0000011
NS00033994
EN300-19631
A831977
Q63396463
F9995-1646
Z104474532
p-Nitrobromobenzene, liquid or solid [UN2732] [Keep away from food]
Solubility of 1-bromo-4-nitro-benzene
The solubility of 1-bromo-4-nitro-benzene (C6H4BrNO2) presents some interesting characteristics due to its unique structure. This compound, a halogenated nitroaromatic, demonstrates varied solubility in different solvents.
Key Points of Solubility:
In summary, while 1-bromo-4-nitro-benzene is poorly soluble in aqueous environments, it exhibits greater compatibility with organic, nonpolar solvents. This reinforces the principle that "like dissolves like," making it essential for chemists to select appropriate solvents for reactions and separations involving this compound.