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[Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone is a complex chemical compound characterized by the presence of a bismuth atom, a 1,4-cyclohexadien-1-yl group, and four ketone functional groups. Its bulky and highly reactive molecular structure endows it with potential applications in various fields, making it a subject of interest for further study and exploration in chemistry and chemical engineering.

23783-80-4

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23783-80-4 Usage

Uses

Used in Organic Synthesis:
[Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone is used as a synthetic building block for the creation of novel organic compounds. Its unique structure and reactivity allow for the development of new molecules with potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science.
Used in Catalysis:
In the field of catalysis, [Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone is used as a catalyst or a catalyst precursor to facilitate various chemical reactions. Its ability to participate in multiple types of reactions, such as oxidation, reduction, and C-C bond formation, makes it a valuable asset in the development of new catalytic processes.
Used in Materials Science:
[Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone is used as a component in the development of advanced materials. Its unique molecular arrangement and reactivity can contribute to the creation of materials with enhanced properties, such as improved conductivity, stability, or mechanical strength, which can be applied in various industries, including electronics, aerospace, and energy.
Used in Chemical Engineering:
In chemical engineering, [Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone is used as a key intermediate in the design and synthesis of complex molecules and materials. Its potential applications in this field include the development of new processes, the improvement of existing ones, and the creation of innovative products with enhanced performance and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 23783-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,8 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23783-80:
(7*2)+(6*3)+(5*7)+(4*8)+(3*3)+(2*8)+(1*0)=124
124 % 10 = 4
So 23783-80-4 is a valid CAS Registry Number.

23783-80-4SDS

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-(3,6-dioxocyclohexa-1,4-dien-1-yl)cyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names Biphenyl-2,5,2',5'-tetraon

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:23783-80-4 SDS

23783-80-4Upstream product

23783-80-4Downstream Products

23783-80-4Relevant academic research and scientific papers

Synthesis of carbazolequinone derivatives as inhibitors of Toxoplasma gondii purine nucleoside phosphorylase

Bouaziz, Zouhair,Gherardi, Arnaud,Regnier, Francois,Sarciron, Marie-Elizabeth,Bertheau, Xavier,Fenet, Bernard,Walchshofer, Nadia,Fillion, Houda

, p. 1834 - 1838 (2007/10/03)

9-Ethyl-6-hydroxycarbazolequinone (9) was synthesized and submitted to a hetero Diels-Alder reaction towards azadienes 10a or 10b to afford the hydroxypyridocarbazole-5,11-diones 11 or 12a,b. A Bracher cyclization applied to compound 12b led to the 9-hydr

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