Interesting facts
Interesting Facts about 1,3-Diisopropylbenzene
1,3-Diisopropylbenzene is an intriguing aromatic hydrocarbon that draws interest from chemists for a couple of reasons:
- Structural Characteristics: The compound features two isopropyl groups attached to the benzene ring at the 1- and 3- positions, giving it a unique symmetry as well as influencing its chemical behavior.
- Application Potential: Its structure lends itself to various applications in the field of organic synthesis and catalysis. Researchers explore its use as a solvent and an intermediate in the manufacture of specialty chemicals.
- Isomeric Diversity: 1,3-Diisopropylbenzene is one of several isomers of diisopropylbenzene, highlighting the importance of positioning in organic chemistry. This variety can lead to differing physical and chemical properties, raising interesting questions about reactivity and synthesis.
- Chemical Reactions: The presence of both aliphatic and aromatic segments allows it to participate in a range of chemical reactions, such as electrophilic aromatic substitution, which can lead to further complex compounds.
- Research Significance: Scientists often study compounds like 1,3-Diisopropylbenzene to understand reaction mechanisms, stability of isomers, and structural effects on reactivity, which are fundamental to organic chemistry.
As noted in the literature, "aromatic hydrocarbons like 1,3-diisopropylbenzene often showcase a delightful interplay of stability and reactivity that can serve as a gateway for exploring more complex organic transformations." This blend of properties makes 1,3-Diisopropylbenzene a fascinating subject of study for both students and professionals in the field.
Synonyms
1,3-DIISOPROPYLBENZENE
99-62-7
m-Diisopropylbenzene
Benzene, 1,3-bis(1-methylethyl)-
Benzene, m-diisopropyl-
1,3-di(propan-2-yl)benzene
1,3-Bis(1-methylethyl)benzene
m-Diisopropylbenzol
3-Isopropylcumene
HSDB 5325
EINECS 202-773-1
BRN 1905828
1,3-bis(propan-2-yl)benzene
DTXSID8026640
meta-Diisopropylbenzene
AI3-08224
482VXW192E
MFCD00008889
CHEMBL31352
3,5-DIISOPROPYLBENZENE
DTXCID006640
EC 202-773-1
1,3-DIISOPROPYLBENZENE [HSDB]
1,?3-?Diisopropylbenzene
CAS-99-62-7
UNII-482VXW192E
mDiisopropylbenzol
mDiisopropylbenzene
Benzene, mdiisopropyl
meta-diisopropyl benzene
1,3-Diisopropyl-benzene
1,3-dipropan-2-ylbenzene
1,3-di-iso-propyl-benzene
1,3Bis(1methylethyl)benzene
1,3-Diisopropylbenzene, 96%
Benzene, 1,3bis(1methylethyl)
UNEATYXSUBPPKP-UHFFFAOYSA-
CHEBI:189570
Benzene, 1,3-di-(1-methylethyl)
Tox21_201318
Tox21_300362
BDBM50409536
AKOS009031313
NCGC00164041-01
NCGC00164041-02
NCGC00164041-03
NCGC00254476-01
NCGC00258870-01
AS-57826
CS-0154284
D0927
D2490
NS00010078
EN300-20928
1-Isopropyl-3-methylbenzene (ACD/Name 4.0)
D97400
Q27259097
InChI=1/C12H18/c1-9(2)11-6-5-7-12(8-11)10(3)4/h5-10H,1-4H3
202-773-1
Solubility of 1,3-Diisopropylbenzene
1,3-Diisopropylbenzene, with the chemical formula C12H18, is known for its unique solubility characteristics.
The solubility of this compound can be summarized with the following key points:
In summary, while 1,3-diisopropylbenzene shows limited solubility in water, it is readily soluble in various organic solvents, making it quite versatile in chemical applications. The specific interactions between molecules in the solvent and solute play a crucial role in determining its solubility behavior.