Interesting facts
Interesting Facts about 2,2,4-trimethyl-1H-quinoline
2,2,4-trimethyl-1H-quinoline is a fascinating compound that belongs to the class of quinoline derivatives, known for their diverse applications in various fields. Here are some notable facts to consider:
- Structural Significance: Quinoline itself is a bicyclic compound, comprising a benzene ring fused to a pyridine ring. The presence of three methyl groups in 2,2,4-trimethyl-1H-quinoline enhances its molecular complexity and affects its chemical behavior.
- Biological Activity: Many quinoline derivatives have shown promise in medicinal chemistry. They are often studied for their potential antimicrobial, antimalarial, and anticancer properties. Thus, 2,2,4-trimethyl-1H-quinoline may warrant further investigation for therapeutic uses.
- Fluorescent Properties: Some quinoline compounds exhibit interesting fluorescence characteristics. This makes them valuable in fields like photochemistry and fluorescent labeling in biological studies.
- Material Science: Quinoline derivatives can influence the physical properties of polymers and other materials, making them significant in materials science.
- Research Applications: Due to its unique structure, 2,2,4-trimethyl-1H-quinoline is a subject of research for developing new chemical syntheses and creating novel functional materials.
In conclusion, the intricate nature of 2,2,4-trimethyl-1H-quinoline provides a rich ground for research and applications, making it a compound worth studying in greater depth. As a scientist or chemistry student, exploring its properties and potential uses could well lead to exciting discoveries!
Synonyms
2,2,4-Trimethyl-1,2-dihydroquinoline
147-47-7
1,2-DIHYDRO-2,2,4-TRIMETHYLQUINOLINE
Quinoline, 1,2-dihydro-2,2,4-trimethyl-
Acetone anil
Flectol H
Acetonanil
2,2,4-trimethyl-1H-quinoline
Agerite resin D
Flectol A
Flectol pastilles
Polnox R
Vulkanox HS/LG
Vulkanox HS/powder
NCI-C60902
Acetone anil (quinoline derivative)
2,2,4-Trimethyl-1,2-dihydroquinone
Trimethyl-1,2-dihydroquinoline
NSC 4175
MFCD00044248
2,2,4-Trimethyl-1,2-dihydrochinolin
DTXSID0025070
1,2-Dihydro-2,2,4-trimethylquinoline (monomer)
NSC-4175
Antioxidant HS
0553M374Q3
Antioxidant HSL
Permanax TQ
Polnoks R
Agerite MA
Antigene RDF
Nonflex RD
Permanax 45
Nocrac 224
Trimethyl dihydroquinoline
CCRIS 4795
CCRIS 4914
Acetone anil (quinoline deriv.)
HSDB 1103
1,2-Dihydro-2,2,4-trimethylquinoline (>85%)
EINECS 205-688-8
Hydroquin
AI3-17714
2,2,4-Trimethyl-1,2-dihydrochinolin [Czech]
UNII-0553M374Q3
TMDQ
Good-rite 3140
Acetonanil (Salt/Mix)
Acetonanyl (Salt/Mix)
ANTIOXIDANT FR-SB
DSSTox_CID_5070
EC 500-051-3
DSSTox_RID_77651
DSSTox_GSID_25071
SCHEMBL44875
MLS002174246
CHEMBL294154
DTXCID605070
ZNRLMGFXSPUZNR-UHFFFAOYSA-
NSC4175
HMS1655H02
HMS3039L13
2,4-Trimethyl-1,2-dihydroquinone
Tox21_201077
Tox21_202467
2,4-Trimethyl-1,2-dihydroquinoline
AKOS000274374
FP40575
SB67449
WLN: T66 BM CHJ C1 C1 E1
NCGC00073733-02
NCGC00073733-03
NCGC00073733-04
NCGC00258630-01
NCGC00260016-01
AS-44332
CAS-147-47-7
FT153116
SMR001261421
SY029873
CAS-26780-96-1
DB-111020
CS-0046816
NS00010679
EN300-57908
A10817
D70537
1,2-Dihydro-2,2,4-trimethylquinoline (85per cent)
1,2-DIHYDRO-2,2,4-TRIMETHYLQUINOLINE [HSDB]
Q27236080
F1974-0002
Poly(1,2-dihydro-2,2,4-trimethylquinoline) Softening point 80-100 degrees C
31014-67-2
InChI=1/C12H15N/c1-9-8-12(2,3)13-11-7-5-4-6-10(9)11/h4-8,13H,1-3H3
Solubility of 2,2,4-trimethyl-1H-quinoline
2,2,4-trimethyl-1H-quinoline exhibits a distinctive solubility profile that aligns with its molecular characteristics. This compound belongs to the class of quinolines, which generally shows varying solubility in different solvents. Here’s an overview of its solubility behavior:
Furthermore, it’s important to note that temperature and pressure can influence the solubility of this compound significantly. As the temperature increases, solubility in certain solvents may enhance, leading to various applications in chemical contexts.
In summary, while 2,2,4-trimethyl-1H-quinoline is more soluble in non-polar environments, it demonstrates limited solubility in polar solutions, making it essential to consider the choice of solvent when working with this compound.