Interesting facts
Interesting Facts About 4-(4-Nitrophenyl)morpholine
4-(4-Nitrophenyl)morpholine is a fascinating organic compound that plays a significant role in various fields of research and application. Here are some intriguing aspects worth noting:
- Versatile Chemical Structure: The compound features both a nitrophenyl group and a morpholine ring, giving it a unique blend of reactivity and stability. This combination is often exploited in synthetic organic chemistry.
- Importance in Medicinal Chemistry: Compounds like 4-(4-nitrophenyl)morpholine are often studied for their potential pharmacological properties. Researchers are continually exploring its effects and mechanisms of action, making it a subject of interest in drug development.
- Applications: This compound can function as a building block for various organic synthesis pathways, serving as an important intermediate in the creation of more complex molecules, including pharmaceuticals and agrochemicals.
- Noteworthy Evidence: Studies have indicated that nitro-substituted compounds can exhibit significant biological activity, including antimicrobial and anticancer properties. This makes 4-(4-nitrophenyl)morpholine a candidate for further investigation in these areas.
- Research Contributions: The presence of the nitro group can also influence the compound’s electronic properties, making it a valuable target for experimental research in understanding reaction mechanisms and kinetic profiles.
In summary, 4-(4-nitrophenyl)morpholine is more than just a chemical compound; it is a notable participant in the broader narrative of chemical research. As scientists and students uncover its various facets, they contribute to the ever-expanding knowledge in fields such as pharmacology, organic synthesis, and materials science.
Synonyms
4-(4-Nitrophenyl)morpholine
10389-51-2
Morpholine, 4-(4-nitrophenyl)-
p-Morpholinonitrobenzene
4-(p-Nitrophenyl)morpholine
4-Morpholinyl nitrobenzene
N-(p-Nitrophenyl)-morpholine
MORPHOLINE, 4-(p-NITROPHENYL)-
EINECS 233-851-3
NSC 27271
BRN 0210854
DTXSID5065061
DTXCID8032833
233-851-3
4-Morpholinonitrobenzene
N-(4-Nitrophenyl)morpholine
4-(4-Nitrophenyl) Morpholine
4-Nitrophenylmorpholine
MFCD00023317
QQ5L4U8QQS
MLS002639157
NSC-27271
Maybridge1_001242
UNII-QQ5L4U8QQS
N-(p-Nitrophenyl)morpholine
SCHEMBL85548
4-(p-Nitrophenyl)-morpholin
4-(4-nitrophenyl)-morpholine
SCHEMBL3282015
4-(4-Nitro-phenyl)-morpholine
CHEMBL1871103
SCHEMBL12247909
SCHEMBL27828925
HMS545A10
IAJDSUYFELYZCS-UHFFFAOYSA-
4-(4-nitrophenyl) (morpholine)
HMS3089J16
ALBB-023290
CS-B0266
NSC27271
BTB 05771
CCG-51799
SBB006371
STK123297
AKOS000446114
AC-7242
MS-2079
SMR001488765
ST057427
SY005309
DB-001572
N1124
NS00023265
SR-01000408777
SR-01000408777-1
SR-01000408777-2
InChI=1/C10H12N2O3/c13-12(14)10-3-1-9(2-4-10)11-5-7-15-8-6-11/h1-4H,5-8H2
Solubility of 4-(4-nitrophenyl)morpholine
The solubility of 4-(4-nitrophenyl)morpholine (C10H12N2O3) displays some intriguing characteristics. Its behavior in various solvents can significantly impact its application in different chemical processes.
In Solvent Solutions:
It is interesting to note that the presence of the nitrophenyl group can also affect solubility behavior by introducing electron-withdrawing effects, thereby influencing intermolecular interactions.
In summary, the solubility of 4-(4-nitrophenyl)morpholine can be characterized by:
Understanding the solubility of this compound is essential for its effective utilization in various chemical applications. As always, empirical testing is advised to quantify solubility in specific solvent systems.