476-34-6
Chemical Structure
Isoindigo
- CAS No.: 476-34-6
- Formula:C16H10N2O2
- Molecular Weight:262.27
IUPAC Name: (E)-[3,3'-biindolinylidene]-2,2'-dione
InChIKey: MLCPSWPIYHDOKG-BUHFOSPRSA-N
SMILES: O=C1NC2=C(C=CC=C2)/C1=C3C(NC4=C\3C=CC=C4)=O
Biological Activity: Isoindigo acts as the acceptor unit in donor-acceptor (D-A) conjugated polymers and belongs to the indigo dye family. Isoindigo contains two lactam rings and exhibits strong electron-withdrawing properties. Isoindigo can be used in dyeing and pigment preparation. Isoindigo shows high mobility and excellent environmental stability in field-effect transistors (FETs). Isoindigo possesses the activity to inhibit tumor cell proliferation and has certain anti-tumor activity[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Isoindigo | 99.67% | Isoindigo acts as the acceptor unit in donor-acceptor (D-A) conjugated polymers and belongs to the indigo dye family. Isoindigo contains two lactam rings and exhibits strong electron-withdrawing properties. Isoindigo can be used in dyeing and pigment preparation. Isoindigo shows high mobility and excellent environmental stability in field-effect transistors (FETs). Isoindigo possesses the activity to inhibit tumor cell proliferation and has certain anti-tumor activity. | ||||||||||||||||||||
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Isoindigo (Standard) | Isoindigo (Standard) is the analytical standard of Isoindigo (HY-107869). This product is intended for research and analytical applications. Isoindigo acts as the acceptor unit in donor-acceptor (D-A) conjugated polymers and belongs to the indigo dye family. Isoindigo contains two lactam rings and exhibits strong electron-withdrawing properties. Isoindigo can be used in dyeing and pigment preparation. Isoindigo shows high mobility and excellent environmental stability in field-effect transistors (FETs). Isoindigo possesses the activity to inhibit tumor cell proliferation and has certain anti-tumor activity. | |||||||||||||||||||||
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References
- [1]. Wee XK,et al. Synthesis and evaluation of functionalized isoindigos as antiproliferative agents. Bioorg Med Chem. 2009 Nov 1;17(21):7562-71. [Content Brief]
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[2]. Romain Stalder, et al. Isoindigo, a Versatile Electron-Deficient Unit For High-Performance Organic Electronics. Chemistry of Materials. October 4, 2013.
- [3]. Lei T, et al. Design, synthesis, and structure-property relationships of isoindigo-based conjugated polymers. Acc Chem Res. 2014;47(4):1117-1126. [Content Brief]
