Interesting facts
Interesting Facts about 1-tert-butyl-3-methyl-benzene
1-tert-butyl-3-methyl-benzene, commonly known as pseudocumene, is a compound that exhibits some fascinating properties and applications within the realm of organic chemistry. Here are some intriguing details:
- Isomeric Structure: This compound is part of the larger family of aromatic hydrocarbons. Its structure features three distinct isomers: o-cumene, m-cumene, and p-cumene. The positioning of the tert-butyl and methyl groups on the benzene ring creates a unique steric environment.
- Industrial Use: Pseudocumene serves as a valuable solvent in various processes, especially in the production of resins and paints. Its properties make it an excellent candidate for applications requiring stability and low reactivity.
- Environmental Aspect: While pseudocumene is an important industrial solvent, it is interesting to note how its environmental impact is continuously studied. Understanding the behavior of such compounds in nature is essential in advancing sustainable practices.
- Boiling Point Elevation: The presence of bulky tert-butyl groups within the molecule enhances its boiling point, showcasing the influence of molecular structure on physical properties - a key concept in physical chemistry.
- Synthesis Routes: Pseudocumene can be synthesized through several methods, including the isomerization of cumene in the presence of acids. This process is an excellent demonstration of organic synthesis techniques for students.
The study of 1-tert-butyl-3-methyl-benzene not only reveals its structural beauty but also emphasizes its practicality in various industrial applications. As Michael Faraday once said, "Nothing is too wonderful to be true, if it be consistent with the laws of nature." This compound exemplifies how nature's laws allow us to engineer complex materials for everyday use.
Synonyms
3-tert-Butyltoluene
RefChem:505413
677-961-3
1075-38-3
1-tert-Butyl-3-methylbenzene
1-(tert-Butyl)-3-methylbenzene
Toluene, m-tert-butyl-
MFCD00059210
Benzene, 1-(1,1-dimethylethyl)-3-methyl-
m-tert-Butyltoluene
1-Methyl-3-tert-butylbenzene
butyltoluol
NSC23700
3-(tert-Butyl)toluene
Benzene,1-(1,1-dimethylethyl)-3-methyl-
SCHEMBL348758
SCHEMBL349313
SCHEMBL887637
SCHEMBL933375
1-methyl-3-tert-butyl-benzene
1-tert-butyl-3-methyl-benzene
SCHEMBL1561562
SCHEMBL1777557
SCHEMBL2869063
SCHEMBL4330647
SCHEMBL6348674
SCHEMBL28141491
SCHEMBL29714909
JTIAYWZZZOZUTK-UHFFFAOYSA-
DTXSID10148068
WLN: 1X1&1&R C1
BAA07538
Benzene,1-dimethylethyl)-3-methyl-
NSC 23700
NSC-23700
AS-77457
SY053396
B0967
Benzene, 1-methyl-3-(1,1-dimethylethyl)-
CS-0318840
NS00113982
3-(2-methyl-2-propyl)-1-methyl-butylbenzene
T70059
InChI=1/C11H16/c1-9-6-5-7-10(8-9)11(2,3)4/h5-8H,1-4H3
Solubility of 1-tert-butyl-3-methyl-benzene
1-tert-butyl-3-methyl-benzene, also known as p-cymene, exhibits specific solubility characteristics largely due to its molecular structure. This compound is predominantly nonpolar, which influences its interaction with various solvents. Here are some key points regarding its solubility:
In summary, 1-tert-butyl-3-methyl-benzene's low water solubility compels it to find greater compatibility with nonpolar environments, making it significantly relevant in various chemical applications where hydrophobic interactions are critical.