Interesting facts
Interesting Facts About 3-Nitrobenzaldehyde
3-Nitrobenzaldehyde, a crucial compound in the realm of organic chemistry, fascinates both scientists and students alike due to its functionality and versatility. Here are some noteworthy aspects:
- Structural Characteristics: This compound features a nitro group (-NO2) attached to the meta position of a benzaldehyde ring. The unique placement of the nitro group significantly influences its reactivity and properties.
- Synthesis: 3-Nitrobenzaldehyde can be synthesized through various methodologies, including nitration of benzaldehyde. This step is essential in the synthesis of other complex organic molecules.
- Applications: It plays a pivotal role in organic synthesis, particularly in the creation of dyes, pharmaceuticals, and agrochemicals. Its derivatives are often employed in constructing larger, more complex chemical structures.
- Reactivity: The electron-withdrawing nature of the nitro group enhances the electrophilic substitution reactions, making it an intriguing subject of study in mechanistic organic chemistry.
- Research and Development: Recently, researchers have been exploring the potential of 3-nitrobenzaldehyde in various applications, including its role as an intermediate in the synthesis of biologically active compounds.
As Linus Pauling once said, "The Science of Chemistry is all about the relationship between the properties of molecules and their behavior." In the case of 3-nitrobenzaldehyde, this relationship is a profound example of how a simple structural modification can lead to a compound of great significance.
Overall, 3-nitrobenzaldehyde exemplifies the beauty of organic chemistry, showcasing how targeted modifications can yield compounds with a myriad of practical applications.
Synonyms
3-NITROBENZALDEHYDE
99-61-6
m-Nitrobenzaldehyde
Benzaldehyde, 3-nitro-
3-Formylnitrobenzene
meta-nitrobenzaldehyde
5-Nitrobenzaldehyde
Benzaldehyde, m-nitro-
3-nitro-benzaldehyde
MFCD00007249
CCRIS 1784
NSC 5504
EINECS 202-772-6
UNII-G4O92KO71Z
G4O92KO71Z
DTXSID8049383
AI3-08906
NSC-5504
3-Nitrobenzenecarboxaldehyde
DTXCID5029342
EC 202-772-6
meta-nitrobenzaldehyde m-nitrobenzaldehyde
mNitrobenzaldehyde
5nitrobenzaldehyde
3Formylnitrobenzene
3-nitrobenzaldehyle
m-nitro-benzaldehyde
Benzaldehyde, mnitro
3-nitro benzaldehyde
Benzaldehyde, 3nitro
3-nitrobenzenealdehyde
(3-nitrophenyl)methanone
WLN: WNR CVH
3-nitrophenylcarboxaldehyde
3-Nitrobenzaldehyde, 99%
SCHEMBL54487
CHEMBL238132
NSC5504
CHEBI:231487
Tox21_202955
BBL011958
STK199270
AKOS000118886
CS-W018126
FN34469
HY-W017410
PS-3388
CAS-99-61-6
NCGC00260501-01
AC-10904
SY001556
3-Nitrobenzaldehyde, ReagentPlus(R), 99%
DB-024310
N0129
NS00001222
EN300-18024
3-Nitrobenzaldehyde, technical, >=95% (GC)
AP-065/40233249
3-Nitrobenzaldehyde, Vetec(TM) reagent grade, 98%
Q2816007
Z57127514
F1294-0141
202-772-6
cyclohexane-1,2-diamine; 5-(1,2-dihydroxyethyl)-3-hydroxy-4-oxo-furan-2-olate; platinum(2+)
Solubility of 3-nitrobenzaldehyde
3-nitrobenzaldehyde, with the chemical formula C7H5NO3, exhibits interesting solubility characteristics that are noteworthy:
In summary, while 3-nitrobenzaldehyde is not very soluble in water, it finds compatibility in several organic solvents, making it versatile for various reactions and applications in organic chemistry. Its solubility is an essential factor to consider when handling and utilizing this compound in laboratory settings.