Interesting facts
Interesting Facts about 1-indolin-1-ylethanone
1-indolin-1-ylethanone is a fascinating compound that belongs to the class of indole derivatives, which are known for their diverse chemical properties and biological activities. Here are some intriguing aspects of this compound:
- Potential Therapeutic Applications: Indole derivatives, including 1-indolin-1-ylethanone, have garnered significant interest in medicinal chemistry due to their potential as drug candidates. They may exhibit activities against various diseases, including cancer and neurological disorders.
- Biological Significance: Compounds containing the indoline structure are often studied for their role in biological pathways. They may act as enzyme inhibitors or modulators of neurotransmitter systems, highlighting their importance in pharmaceutical research.
- Synthesis: The synthesis of 1-indolin-1-ylethanone is an area that has attracted attention. Researchers explore different synthetic routes to optimize yield and purity, and the reactions often involve innovative methodologies that underscore the creativity in organic chemistry.
- Structure-Activity Relationship (SAR): Understanding how the structural features of 1-indolin-1-ylethanone influence its biological properties is crucial. This fits into the broader context of drug design, where subtle changes to the molecular structure can lead to significant alterations in biological activity.
In summary, 1-indolin-1-ylethanone is not just a compound; it is a gateway into the multidisciplinary realm of medicinal chemistry, showcasing how a singular structure can hold potential leads for innovative treatments and significant biological interactions. As chemists delve deeper into its properties, the outlook for this compound remains bright.
Synonyms
1-Acetylindoline
1-(2,3-dihydro-1H-indol-1-yl)ethan-1-one
881-370-8
16078-30-1
1-(indolin-1-yl)ethanone
N-Acetylindoline
1-(2,3-dihydroindol-1-yl)ethanone
MFCD00022908
1H-Indole, 1-acetyl-2,3-dihydro-
acetylindoline
Ethanone, 1-(2,3-dihydro-1H-indol-1-yl)-
CHEMBL3274978
1-(2,3-dihydro-indol-1-yl)-ethanone
INDOLINE, 1-ACETYL-
BRN 0129366
1H-Indole, 1-acetyl-2,3-dihydro- (9CI)
1-acetyl-indoline
1-ACETYL-2,3-DIHYDROINDOLE
1-indolin-1-ylethanone
Maybridge1_005081
1-Acetylindoline, 98%
ChemDiv2_000149
5-20-06-00242 (Beilstein Handbook Reference)
SCHEMBL396037
SCHEMBL1165734
SCHEMBL2224344
SCHEMBL3459392
SCHEMBL3838004
SCHEMBL3838005
SCHEMBL6000060
1-(indolin-1-yl)ethan-1-one
SCHEMBL15009454
SCHEMBL25392290
SCHEMBL29449723
HMS555O21
DTXSID10166984
HMS1369G17
HMS5088M03
1-Acetyl-2,3-dihydro-1H-indole
BDBM50016624
STK364320
AKOS003239122
CS-W010870
FA52418
SB64066
AC-23381
SY015454
1-(2,3-dihydro-1H-indol-1-yl)ethanone
1-(2,3-dihydro-1H-indol-1-yl)-ethanone
DB-043468
ST45025043
EN300-49295
SR-01000389835
SR-01000389835-1
Z30624388
F0451-0187
1-(2,3-Dihydro-1H-indol-1-yl)ethan-1-one;1-Acetyl-2,3-dihydroindole
InChI=1/C10H11NO/c1-8(12)11-7-6-9-4-2-3-5-10(9)11/h2-5H,6-7H2,1H
Solubility of 1-Indolin-1-ylethanone
1-Indolin-1-ylethanone, with the chemical formula C10H9N1O1, exhibits notable solubility characteristics that are essential to its applications in various fields. When considering the solubility of this compound, several factors come into play:
In summary, while 1-Indolin-1-ylethanone is relatively soluble in non-polar organic solvents, its hydrophobic nature leads to poor solubility in polar solvents like water. Understanding these solubility properties is vital for optimizing its use in chemical reactions and formulations.