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2,6-Diacetoxy-9,10-anthraquinone is a chemical compound with the molecular formula C20H14O6, belonging to the anthraquinone family of naturally occurring compounds found in various plants. This specific derivative is characterized by its red to brown solid form, a distinctive odor, and its solubility in organic solvents rather than water. It is recognized for its vibrant color properties and potential medicinal applications.

1747-94-0

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1747-94-0 Usage

Uses

Used in Textile Industry:
2,6-Diacetoxy-9,10-anthraquinone is used as a dye in the textile industry for its ability to impart vibrant colors to fabrics. Its colorfastness and compatibility with various textile materials make it a valuable component in the production of dyed textiles.
Used in Ink and Paint Production:
In the ink and paint industries, 2,6-Diacetoxy-9,10-anthraquinone is used as a precursor in the production of dyes and pigments, contributing to the creation of a wide range of colorants for different applications, from artistic to industrial uses.
Used in Pharmaceutical Research:
2,6-Diacetoxy-9,10-anthraquinone is studied for its potential medicinal properties, particularly as an anti-cancer agent. Its chemical structure and biological activity are being investigated for possible therapeutic applications in oncology, highlighting its dual role as both an industrial chemical and a candidate for pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 1747-94-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1747-94:
(6*1)+(5*7)+(4*4)+(3*7)+(2*9)+(1*4)=100
100 % 10 = 0
So 1747-94-0 is a valid CAS Registry Number.

1747-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-acetyloxy-9,10-dioxoanthracen-2-yl) acetate

1.2 Other means of identification

Product number -
Other names 2,6-Diacetoxy-anthrachinon

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:1747-94-0 SDS

1747-94-0Relevant academic research and scientific papers

Self-assembled boronic ester cavitand capsule as a photosensitizer and a guard nanocontainer against photochemical reactions of 2,6-diacetoxyanthracene

Nishimura, Naoki,Kobayashi, Kenji

experimental part, p. 6079 - 6085 (2010/11/04)

Figure presented. The optical properties of 2,6-diacetoxyanthracene 4 encapsulated in the self-assembled boronic ester cavitand capsule 3 in C 6H6 are described. Upon excitation at 285 nm, the encapsulated 4 showed strong fluorescence emission as a result of the energy transfer from the excited 3 to the encapsulated 4, while 4 alone in C 6H6 exhibited very weak emission. Upon photoirradiation at 365 nm, the encapsulated 4 also showed strong fluorescence emission and remained almost intact, whereas 4 alone in C6H6 gradually underwent photodimerization and photooxygenation to afford photodimers 5 and 5′ and 9,10-anthraquinone 6 via 9,10-endoperoxide 7, respectively. Thus, the capsule 3 serves as a photosensitizer for the encapsulated 4 as well as a guard nanocontainer to protect against the photochemical reactions of 4.

Guest-encapsulation properties of a self-assembled capsule by dynamic boronic ester bonds

Nishimura, Naoki,Yoza, Kenji,Kobayashi, Kenji

supporting information; experimental part, p. 777 - 790 (2010/04/01)

Two molecules of tetrakis(dihydroxyboryl)-cavitand 1a as an aromatic cavity and four molecules of 1,2-bis(3,4-dihydroxyphenyl)ethane 2 as an equatorial linker self-assemble into capsule 3a via the formation of eight dynamic boronic ester bonds in CDClsub

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