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(1-[2-(diethylamino)ethyl]amino-9-oxo-9H-thioxanthen-4-yl)methyl acetate is a synthetic compound that features a thioxanthene core structure with an amine and acetate functional group. (1-[2-(diethylamino)ethyl]amino-9-oxo-9H-thioxanthen-4-yl)methyl acetate is known for its unique chemical properties, which include its use as a fluorescent tracer in various scientific applications.

3612-72-4

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3612-72-4 Usage

Uses

Used in Bioimaging and Cell Labeling Studies:
(1-[2-(diethylamino)ethyl]amino-9-oxo-9H-thioxanthen-4-yl)methyl acetate is utilized as a fluorescent tracer for bioimaging and cell labeling studies. Its fluorescent properties make it a valuable tool for visualizing cellular structures and tracking cellular processes in research.
Used as a pH-Sensitive Fluorescent Dye:
In the field of chemical biology, (1-[2-(diethylamino)ethyl]amino-9-oxo-9H-thioxanthen-4-yl)methyl acetate is used as a pH-sensitive fluorescent dye. The presence of the diethylamino group allows the compound to respond to changes in pH, making it useful for pH-dependent imaging applications and studies involving cellular environments with varying pH levels.
Used in Organic Electronic Devices:
(1-[2-(diethylamino)ethyl]amino-9-oxo-9H-thioxanthen-4-yl)methyl acetate has been investigated for its potential use in organic electronic devices. Its unique chemical structure and properties make it a candidate for applications in the development of advanced electronic materials and devices.
Used as a Photosensitizer in Photodynamic Therapy:
In the medical field, specifically in cancer treatment, (1-[2-(diethylamino)ethyl]amino-9-oxo-9H-thioxanthen-4-yl)methyl acetate has been explored as a photosensitizer for photodynamic therapy. This application takes advantage of the compound's ability to absorb light and generate reactive oxygen species, which can be used to target and destroy cancer cells.
Used in Chemistry, Biology, and Materials Science Research:
(1-[2-(diethylamino)ethyl]amino-9-oxo-9H-thioxanthen-4-yl)methyl acetate is a versatile compound that exhibits a range of applications across various scientific disciplines. It is used in research and development within the fields of chemistry, biology, and materials science to advance knowledge and create innovative applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3612-72-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3612-72:
(6*3)+(5*6)+(4*1)+(3*2)+(2*7)+(1*2)=74
74 % 10 = 4
So 3612-72-4 is a valid CAS Registry Number.

3612-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-[2-(diethylamino)ethylamino]-9-oxothioxanthen-4-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names -

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:3612-72-4 SDS

3612-72-4Downstream Products

3612-72-4Relevant academic research and scientific papers

Preparation and antischistosomal and antitumor activity of hycanthone and some of its congeners. Evidence for the mode of action of hycanthone

Archer,Pica-Mattoccia,Cioli,Seyed-Mozaffari,Zayed

, p. 254 - 260 (2007/10/02)

The synthesis of a series of esters of hycanthone (HC) and 7-hydroxyhycanthone, their antitumor activity, and their antischistosomal effects on HC-sensitive and HC-resistant schistosomes are reported. Binding studies using tritium-labeled HC and hycanthon

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