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56289-67-9

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  • 2-[2-[2-CHLORO-3-[2-(1,3-DIHYDRO-1,3,3-TRIMETHYL-2H-INDOL-2-YLIDENE)-ETHYLIDENE]-1-CYCLOHEXEN-1-YL]-VINYL]-1,3,3-TRIMETHYL-3H-INDOLIUM IODIDE

    Cas No: 56289-67-9

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  • 2-[2-[2-chloro-3-[(1,3-dihydro-1,3,3-trimethyl-2H-indol-2-ylidene)-ethylidene]-1-cyclohexen-1-yl]ethenyl]-1,3,3-trimethylindolium iodide

    Cas No: 56289-67-9

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56289-67-9 Usage

General Description

2-[2-[2-CHLORO-3-[(1,3-DIHYDRO-1,3,3-TRIMETHYL-2 H-INDOL-2-YLIDENE) ETHYLIDENE]-1-CYCLOHEXEN-1-YL]ETHENYL]-1,3,3-TRIMETHYLINDOLIUM IODIDE is a chemical compound with a complex molecular structure. It contains a quaternary ammonium cation, specifically a 1,3,3-trimethylindolinium cation, and an iodide anion. The compound also features a chloro-substituted cyclohexene ring and a 1,3-dihydro-1,3,3-trimethyl-2H-indol-2-ylidene group. This chemical is commonly used in organic synthesis and pharmaceutical research due to its unique structure and potential biological activity. However, it is important to handle and use this compound with caution due to its potentially hazardous nature.

Check Digit Verification of cas no

The CAS Registry Mumber 56289-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,8 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56289-67:
(7*5)+(6*6)+(5*2)+(4*8)+(3*9)+(2*6)+(1*7)=159
159 % 10 = 9
So 56289-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C32H36ClN2.HI/c1-31(2)24-14-7-9-16-26(24)34(5)28(31)20-18-22-12-11-13-23(30(22)33)19-21-29-32(3,4)25-15-8-10-17-27(25)35(29)6;/h7-10,14-21H,11-13H2,1-6H3;1H/q+1;/p-1

56289-67-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-CHLORO-3-[(1,3-DIHYDRO-1,3,3-TRIMETHYL-2 H-INDOL-2-YLIDENE) ETHYLIDENE]-1-CYCLOHEXEN-1-YL]ETHENYL]-1,3,3-TRIMETHYLINDOLIUM IODIDE

1.2 Other means of identification

Product number -
Other names 2-[2-[2-Chloro-3-[(1,3-dihydro-1,3,3-trimethyl-2H-indol-2-ylidene)ethylidene]-1-cyclopenten-1-yl]ethenyl]-1,3,3-trimethylindolium iodide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56289-67-9 SDS

56289-67-9Downstream Products

56289-67-9Relevant articles and documents

ALP-activated probe for diagnosis of liver injury by multispectral optoacoustic tomography

Wu, Yinglong,Zeng, Fang,Sun, Lihe,Chen, Junjie,Wu, Shuizhu

, p. 301 - 330 (2021)

In this chapter, we highlight the advantages of multispectral optoacoustic tomography (MSOT) technique and the activatable photoacoustic probes in the biomedical field, and give a brief introduction to enzyme-activated probes for disease diagnosis and therapeutic outcome evaluation. We also present a detailed description of the procedures for the synthesis of an activatable small molecule probe C1X-OR1 and confirmation of its specific response to alkaline phosphatase in solution and cells. With MSOT, the liposomal C1X-OR1 can be utilized for detection of hepatic ALP as well as for in vivo diagnosis of drug-induced liver injury in a three-dimensional manner.

Optimized Fluorescent Probe for Specific Imaging of Glutathione S-Transferases in Living Cells and Mice

Chen, Hui,Feng, Tian,Gai, Shouchang,Li, Xinxin,Shen, Xin,Song, Aiguo,Wei, Haiqing

, (2020)

GSTP1 has been considered to be a marker for malignancy in many tissues. However, the existing GST fluorescent probes are unfavorable for in vivo imaging because of the limited emission wavelength or insufficient fluorescence enhancement (six-fold). The limited fluorescence enhancement of GST fluorescent probes is mainly ascribed to the high background signals resulting from the spontaneous reaction between GSH and the probes. In this work, a highly specific GST probe with NIR emission has been successfully developed through optimization of the essential unit of the probe to repress the spontaneous reaction. The novel GST probe exhibits over 100-fold fluorescence enhancement upon incubation with GSTP1/GSH and high selectivity over other potential interference. In addition, the probe has been proved to be capable of tracking endogenous GST in A549 cells. Finally, the in vivo imaging results demonstrate that the probe can be used for effective imaging of endogenous GST activity in subcutaneous tumor mouse with high contrast.

Substitution nitrogen for chlorine of heptamethine cyanines for large Stokes shift fluorescent probes

Zheng, Lihui,Wang, Liqiu,Wang, Pengjun,Sun, Qi,Liu, Xuelong,Zhang, Xiaobo,Qiu, Shaobo

, p. 932 - 936 (2016)

On the basis of syntheses of three heptamethine indocyanines with methyl, ethyl, or p-carboxybenzyl groups on N atoms in the indole rings, nine novel aminoderivatives were designed and synthesized by butylamine, taurine, or benzylamine reacting with the indocyanines for substitution nitrogen for chlorine. The obtained products were purified by SiO2 column chromatography, and confirmed by ESI-MS and 1H NMR. Compared to the parents, the aminoderivatives showed blue shifts, larger Stokes shifts, and stronger fluorescence intensity, which were mainly related to the electron-donating ability of the amino substituents in the aminoderivatives. The stronger electron-donating ability of the amino substituents made the maximum absorption wavelengths show greater blue shifts.

A NIR fluorescent probe for the detection of fluoride ions and its application in in vivo bioimaging

Yang, Qiuyun,Jia, Chunman,Chen, Qing,Du, Wei,Wang, Yile,Zhang, Qi

, p. 2002 - 2009 (2017)

A novel near-infrared (NIR) fluorescent probe for the detection of fluoride ions has been developed, which is based on the F-triggered cleavage reaction of the Si-O bond. This probe exhibits excellent selectivity and sensitivity towards fluoride ions. The results of bioimaging experiments with HepG2 cells and mice show that the fluoride probe is available for visualizing exogenous fluoride ions in vitro and in vivo.

New cationic heptamethinecyanine-graphene hybrid materials

Prousis, Kyriakos C.,Canton-Vitoria, Ruben,Pagona, Georgia,Goulielmaki, Maria,Zoumpourlis, Vassilis,Tagmatarchis, Nikos,Calogeropoulou, Theodora

, (2019/12/27)

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