Interesting facts
Interesting Facts About 4-Isopropylaniline
4-Isopropylaniline, a derivative of aniline, is an intriguing compound that serves several critical roles in organic chemistry and industrial applications. Here are some captivating aspects about this compound:
- Structure and Substitution: The presence of the isopropyl group makes 4-isopropylaniline a member of the substituted aniline family, enhancing its solubility and reactivity compared to its parent compound, aniline.
- Applications in Synthetic Chemistry: 4-Isopropylaniline is often used as a building block in the synthesis of various pharmaceuticals, dyes, and other organic compounds, demonstrating its versatility in organic reactions.
- Role in Dye Manufacturing: This compound plays a significant role in the textile industry, wherein it is utilized in the production of azo dyes, responsible for creating vibrant colors in fabrics.
- Research Importance: In the field of organic synthesis, 4-isopropylaniline is a popular subject of study due to its potential to serve as an intermediate in complex molecular transformations and the development of novel materials.
Overall, 4-Isopropylaniline exemplifies how a simple substitution in molecular structure can yield a compound with vast applications and importance in both research and industry. As researchers continue to explore its properties and potential uses, the compound remains a significant player in the realm of organic chemistry.
Synonyms
4-ISOPROPYLANILINE
99-88-7
Cumidine
4-Aminocumene
p-Isopropylaniline
p-Cumidine
4-Amino-1-isopropylbenzene
4-(Propan-2-Yl)Aniline
PARA-ISOPROPYLANILINE
4-propan-2-ylaniline
Benzenamine, 4-(1-methylethyl)-
Cumene, p-amino-
Aniline, p-isopropyl-
4-(2-propyl)aniline
4-(1-methylethyl)aniline
.beta.-(4-Aminophenyl)propane
1-Amino-4-isopropylbenzene
NSC 7198
beta-(4-Aminophenyl)propane
4-(1-Methylethyl)benzenamine
4-isopropyl-aniline
0D54T7V7XL
4-isopropylbenzenamine
4-isopropylphenylamine
CUMIDINE [MI]
NSC-7198
EINECS 202-797-2
MFCD00007900
4-AMINOISOPROPYLBENZENE
AI3-04696
CHEBI:43405
DTXSID20243932
EC 202-797-2
(4-(1-METHYLETHYL)PHENYL)AMINE
cumidin
UNII-0D54T7V7XL
pCumidine
p-Aminocumene
4Aminocumene
pIsopropylaniline
4isopropylaniline
Cumene, pamino
iso-nLc8Cer
4-i-propylaniline
Aniline, pisopropyl
4-iso-propylaniline
4-isopropanylaniline
Cumidine (8CI)
4Amino1isopropylbenzene
4-isopropyl-phenylamine
aniline, 4-isopropyl-
beta(4Aminophenyl)propane
4-(1-Methylethyl)a0ine
4(1Methylethyl)benzenamine
4-Isopropylaniline, 99%
SCHEMBL5955
4-(1-Methylethyl)-aniline
Benzenamine, 4(1methylethyl)
LRTFPLFDLJYEKT-UHFFFAOYSA-
DTXCID50166423
NSC7198
BCP22014
STR01136
STL164349
AKOS000119635
AC-3325
CS-W020082
DB02114
PS-5289
BP-21269
DB-080640
I0371
NS00010898
EN300-19996
D71250
doi:10.14272/LRTFPLFDLJYEKT-UHFFFAOYSA-N.1
4-Isopropylaniline, PESTANAL(R), analytical standard
Q27093183
F2190-0423
Z104476320
InChI=1/C9H13N/c1-7(2)8-3-5-9(10)6-4-8/h3-7H,10H2,1-2H3
202-797-2
682-629-6
Solubility of 4-isopropylaniline
The solubility of 4-isopropylaniline, also known as p-isopropylaniline, can be influenced by several factors. Generally, this compound is a member of the aniline family and is characterized by its unique hydrophobic isopropyl group. Here are some key aspects to consider regarding its solubility:
In summary, the solubility of 4-isopropylaniline is limited in water but is appreciable in most organic solvents. As a result, scientists often utilize this compound in organic reactions where non-aqueous conditions are preferred. The balance between its polar and nonpolar characteristics defines its solubility profile, making it an interesting compound to study in the context of solubility and reactivity.