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1,4,5,8-tetramethylanthracene-9,10-dione, also known as dimethyl-1,4,5,8-anthracenetetrone, is a chemical compound with the molecular formula C20H16O2. It is a bright yellow crystal that is used as a precursor in the synthesis of various organic compounds and dyes.
Used in Organic Chemistry Research:
1,4,5,8-tetramethylanthracene-9,10-dione is used as a reagent for the formation of carbon-carbon bonds and as a building block for the synthesis of more complex molecules.
Used in Organic Compounds and Dyes Synthesis:
1,4,5,8-tetramethylanthracene-9,10-dione is used as a precursor in the synthesis of various organic compounds and dyes.
Used in Organic Light-Emitting Diodes (OLEDs) Development:
1,4,5,8-tetramethylanthracene-9,10-dione is used in the development of organic light-emitting diodes (OLEDs) due to its interesting photophysical properties.
Note: 1,4,5,8-tetramethylanthracene-9,10-dione is also known to be a skin and eye irritant, and proper handling and safety precautions should be observed when working with it in a laboratory setting.

17538-63-5

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17538-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17538-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,3 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17538-63:
(7*1)+(6*7)+(5*5)+(4*3)+(3*8)+(2*6)+(1*3)=125
125 % 10 = 5
So 17538-63-5 is a valid CAS Registry Number.

17538-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,5,8-tetramethylanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,4,5,8-Tetramethyl-9,10-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:17538-63-5 SDS

17538-63-5Relevant academic research and scientific papers

Triptycene based luminescent metal-organic gels for chemosensing

Barman, Samir,Anand Garg, Jai,Blacque, Olivier,Venkatesan, Koushik,Berke, Heinz

, p. 11127 - 11129 (2012)

We report a novel luminescent Al-based metal-organic gel G1 comprising 1,4,5,8-triptycenetetracarboxylic acid, which exhibits highly sensitive detection towards nitro aromatic compounds particularly picric acid. Furthermore, under identical reaction conditions, using a Co(ii) salt instead, a novel 3D framework material, trip-MOF-1, was isolated and its sensitivity towards picric acid was also evaluated.

1,4,7,10-TETRAMETHYL-5,6-DIDEHYDRODIBENZOCYCLOOCTENE. A PRESUMABLY PLANAR FULLY CONJUGATED EIGHT-MEMBERED RING COMPOUND.

Huang, Nai Zheng,Jia, Jian Hua,Wang, Li Li,Chan, Tze-Lock,Mak, Thomas C. W.

, p. 4797 - 4800 (1982)

The first known stable crystalline derivative of 5,6-didehydrodibenzocyclooctene (1), namely, 1,4,7,10-tetramethyl-5,6-didehydrodibenzocyclooctene (2), was prepared and unequivocally characterised.

A STABLE DERIVATIVE OF CYCLOOCTATRIENYNE. SYNTHESIS AND CRYSTAL STRUCTURES OF 1,4,7,10-TETRAMETHYL-5,6-DIDEHYDRODIBENZOCYCLOOCTENE AND 1,4,7,10-TETRAMETHYLDIBENZOCYCLOOCTENE

Chan, Tze-Lock,Mak, Thomas C. W.,Poon, Chi-Duen,Wong, Henry N. C.,Jia, Jian Hua,Wang, Li Li

, p. 655 - 662 (2007/10/02)

A stable derivative of cyclooctatrienyne (1), namely 1,4,7,10-tetramethyl-5,6-didehydrodibenzocyclooctene (3) has been synthesized and fully characterized.X-Ray crystallographic analyses indicate that 3 adopts a "butterfly" conformation intermediate between those of virtually planar 5,6-didehydrodibenzocyclooctene (2) and tub-shaped 1,4,7,10-tetramethyldibenzocyclooctene (16).The methyl substituents effectively shield the otherwise rather exposed strained triple bond of 3 and kinetically stabilize it against dimerization and/or oxidation.

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