Indolines
Indolines are a class of heterocyclic compounds characterized by the presence of an indole ring, which consists of a benzene ring fused to a pyrrole ring. These molecules are known for their diverse chemical and biological properties, making them of significant interest in both academic research and pharmaceutical applications.
Structurally, indolines can vary based on the substitution pattern on the indole ring. Common substituents include methyl groups, hydroxyl, amino, and carboxylic acid functionalities. Due to their structural flexibility, indolines exhibit a wide range of biological activities, including potential use as antiviral agents, anticancer drugs, and neuroprotective compounds.
Indolines are often synthesized through multistep organic reactions such as condensation, ring closure, and functional group manipulation. Their synthesis methods can be optimized for the desired substituents to tailor their properties for specific applications.
In summary, indolines represent a versatile class of heterocycles with promising potential in various fields, including medicinal chemistry, materials science, and natural product research.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
![]() |
7-chloro-2,3-dihydro-1H-indole-2,3-dione | 7477-63-6 | C8H4ClNO2 |
![]() |
Spiro[3H-indole-3,4'-piperidin]-2(1H)-one, 5-bromo- | 920023-50-3 | C12H13BrN2O |
![]() |
4-Benzyloxy-2,3-dihydro-1H-indole | 885278-77-3 | C15H15NO |
![]() |
5-Hydroxyindolin-2-one | 3416-18-0 | C8H7NO2 |
![]() |
4-(2-Hydroxyethyl)-1,3-dihydro-2H-indolin-2-one | 139122-19-3 | C10H11NO2 |
![]() |
1,3,4a,5,9b-Hexahydro,ethylester,2H-pyrido4,3-bindole-2-carboxylicacid | 199725-38-7 | C14H18N2O2 |
![]() |
7-fluoro-2,3-dihydro-1H-indol-2-one | 71294-03-6 | C8H6FNO |
![]() |
Des-N-(2-Diethylaminoethyl)amide Sunitinib Acid | 356068-93-4 | C16H13FN2O3 |
![]() |
6-Bromooxindole | 99365-40-9 | C8H6BrNO |
![]() |
4-bromo-2,3-dihydro-1H-indol-2-one | 99365-48-7 | C8H6BrNO |
Related Literature
-
Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
-
2. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
-
Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
-
Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
-
Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
Recommended suppliers
-
上海帛亦醫(yī)藥科技有限公司Factory Trade Brand reagentsCompany nature: Private enterprises
-
Shenzhen GeneSeqTools Bioscience & Technology Co. Ltd.Factory Trade Brand reagentsCompany nature: Private enterprises
-
Jiangxi Boyang Pharmaceutical Chemical Co., LtdFactory Trade Brand reagentsCompany nature: Private enterprises
-
鉅瀾化工科技(青島)有限公司Factory Trade Brand reagentsCompany nature: Private enterprises
-
Jinta Yudi Pharmaceutical Technology Co., Ltd.Factory Trade Brand reagentsCompany nature: Private enterprises
Recommended products









