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2-Azidoanthraquinone is a chemical compound with the molecular formula C14H7N3O2, characterized by the presence of an anthraquinone core, which is a fused ring system consisting of three benzene rings, and an azide group (N3) attached to the 2-position of the anthraquinone. This yellow crystalline solid is primarily used as a photosensitizer in photodynamic therapy, where it generates reactive oxygen species upon light activation, leading to the destruction of target cells. It is also employed as a chemical intermediate in the synthesis of various dyes and pigments, as well as in the study of photochemical reactions. Due to its potential applications in medicine and industry, 2-azidoanthraquinone is a subject of ongoing research to explore its properties and optimize its use.

49545-73-5

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49545-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49545-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 49545-73:
(7*4)+(6*9)+(5*5)+(4*4)+(3*5)+(2*7)+(1*3)=155
155 % 10 = 5
So 49545-73-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H7N3O2/c15-17-16-8-5-6-11-12(7-8)14(19)10-4-2-1-3-9(10)13(11)18/h1-7H

49545-73-5SDS

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-azidoanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 2-Azidoanthrachinon

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:49545-73-5 SDS

49545-73-5Upstream product

49545-73-5Relevant academic research and scientific papers

Photochemical modification of polyethylene surface with aryl azides

Budruev,Sinjagina

, p. 237 - 241 (2013)

It has been shown that the formation of a covalently grafted modifying layer takes place during the photolysis of polycrystalline layers of 2-azidoanthraquinone and 4-azidobenzoyl azide on the surface of polyethylene. Its thickness is determined by the amount of the azide applied, and phenyl isocyanate groups formed by the photolysis of 4-azidobenzoyl azide are prone to further functionalization of the modified surface with primary amines.

Synthesis and complexation study of new ExTTF-based hosts for fullerenes

Iden, Hassan,Fontaine, Frederic-Georges,Morin, Jean-Francois

supporting information, p. 4117 - 4123 (2014/06/10)

A new series of exTTF hosts has been synthesized for supramolecular binding study of fullerenes C60 and C70. Binding constants for C60 in chlorobenzene, toluene, toluene-CH2Cl2 and CS2 have been calculated for different hosts and a direct structure-affinity relationship has been established. As predicted, receptors with two exTTF moieties (1, 3 and 4) have demonstrated higher binding abilities toward C70 than C60. Depending on the linker used to attach the exTTF unit to the core of the host, different binding modes (1:1 and 2:1) have been obtained. This journal is the Partner Organisations 2014.

A fast and efficient method for the preparation of aryl azides using stable aryl diazonium silica sulfates under mild conditions

Zarei, Amin,Hajipour, Abdol R.,Khazdooz, Leila,Aghaei, Hamidreza

experimental part, p. 4443 - 4445 (2009/11/30)

An efficient, fast, and straightforward procedure for the synthesis of aromatic azides using aryl diazonium silica sulfates and sodium azide at room temperature under mild conditions is described. The use of inexpensive materials, simple and clean work-up

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