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1747-94-0

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1747-94-0 Usage

General Description

2,6-Diacetoxy-9,10-anthraquinone is a chemical compound with the molecular formula C20H14O6. It is a derivative of anthraquinone, which is a naturally occurring compound found in many plants. This specific derivative is often used as a dye and as a precursor in the production of dyes and pigments. It is a red to brown solid with a characteristic odor, and is insoluble in water but soluble in organic solvents. It has been used in the textile industry for its vibrant color properties, and also has applications in the production of inks, paints, and other colorants. Additionally, it has been studied for its potential medicinal properties, including its potential as an anti-cancer agent.

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 articles and documents

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.

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