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7H-benzo[c]thioxanthen-7-one is a chemical compound with the molecular formula C17H11OS. It belongs to the class of benzothioxanthene derivatives, which are heterocyclic organic compounds containing a benzene ring fused to a thioxanthene ring. This particular compound features a carbonyl group (C=O) at the 7-position, which contributes to its chemical reactivity and properties. It is often used as a building block in the synthesis of various organic compounds, including dyes, pigments, and pharmaceuticals. Due to its unique structure, 7H-benzo[c]thioxanthen-7-one exhibits interesting photophysical and electronic properties, making it a subject of interest in the field of organic chemistry and materials science.

3604-44-2

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3604-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3604-44-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3604-44:
(6*3)+(5*6)+(4*0)+(3*4)+(2*4)+(1*4)=72
72 % 10 = 2
So 3604-44-2 is a valid CAS Registry Number.

3604-44-2SDS

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 benzo[c]thioxanthen-7-one

1.2 Other means of identification

Product number -
Other names 7H-Benzo<c>thioxanthen-7-on

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:3604-44-2 SDS

3604-44-2Downstream Products

3604-44-2Relevant academic research and scientific papers

π-Expanded Thioxanthones – Engineering the Triplet Level of Thioxanthone Sensitizers for Lanthanide-Based Luminescent Probes with Visible Excitation

Dansholm, Charlotte Nybro,Junker, Anne Kathrine R.,Nielsen, Lea G.,Kofod, Nicolaj,Pal, Robert,S?rensen, Thomas Just

, p. 1778 - 1788 (2019/07/15)

Bright lanthanide based probes for optical bioimaging must rely on the antenna principle, where the lanthanide-centred excited state is formed by a complex sensitization process. Efficient sensitization of lanthanide-centred emission occurs via triplet states centred on the sensitizing chromophore. Here, the triplet state of thioxanthone chromophores is modulated by extending the π-system. Three thioxanthone chromophores-thioxanthone, benzo[c]thioxanthone, and naphtho[2,3-c]thioxanthone were synthesised and characterised. The triplet state energies and lifetimes is found to change as expected, and two dyes are found to be suitable sensitizers for europium(iii) luminescence. Reactive derivatives of thioxanthone and benzo[c]thioxanthone were prepared and coupled to a 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (DO3A) lanthanide binding pocket. The photophysics and the performance in optical bioimaging of the resulting europium(iii) complexes were investigated. It is concluded that while the energetics favour efficient sensitization, the solution structure does not. While it was found that the complexes are too lipophilic to be efficient luminescent probes for optical bioimaging, we successfully demonstrated bioimaging using europium(iii) luminescence following 405 nm excitation.

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