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2,5-Bis(methoxycarbonyl)-3,4-diphenylcyclopentadienone is a complex organic compound that belongs to the class of chemical structures known as cyclopentadienones, which are a type of carbocyclic compounds. It features a cyclopentadienone core with two methoxycarbonyl groups and is substituted at positions 3 and 4 with phenyl groups. The systematic chemical name for 2,5-BIS(METHOXYCARBONYL)-3,4-DIPHENYLCYCLOPENTADIENONE is 2,5-dimethoxycarbonyl-3,4-diphenylcyclopentadienone, and its molecular formula is C23H18O4. The physical and chemical properties of 2,5-BIS(METHOXYCARBONYL)-3,4-DIPHENYLCYCLOPENTADIENONE, such as density, boiling point, solubility, and safety considerations, may vary depending on the production methods and the purity of the sample.

16691-79-5

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16691-79-5 Usage

Uses

Currently, there is no specific information provided in the materials about the uses of 2,5-Bis(methoxycarbonyl)-3,4-diphenylcyclopentadienone. However, given its complex structure and the fact that it belongs to the cyclopentadienone class, it is likely that 2,5-BIS(METHOXYCARBONYL)-3,4-DIPHENYLCYCLOPENTADIENONE may have potential applications in various fields such as pharmaceuticals, materials science, or as an intermediate in the synthesis of other organic compounds. Further research and development would be required to explore and confirm its specific uses in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 16691-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,9 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16691-79:
(7*1)+(6*6)+(5*6)+(4*9)+(3*1)+(2*7)+(1*9)=135
135 % 10 = 5
So 16691-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H16O5/c1-25-20(23)17-15(13-9-5-3-6-10-13)16(14-11-7-4-8-12-14)18(19(17)22)21(24)26-2/h3-12H,1-2H3

16691-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-oxo-4,5-diphenylcyclopenta-3,5-diene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3,4-Diphenylcyclopentadienone-2,5-dicarboxylic Acid Dimethyl Ester

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:16691-79-5 SDS

16691-79-5Downstream Products

16691-79-5Relevant academic research and scientific papers

Synthesis, Molecular Packing, and Thin Film Transistors of Dibenzo[a,m]rubicenes

Gu, Xiao,Xu, Xiaomin,Li, Huiyan,Liu, Zhifeng,Miao, Qian

supporting information, p. 16203 - 16208 (2016/01/15)

We herein report an efficient synthesis of dibenzo[a,m]rubicene, a new member of nonplanar cyclopenta-fused polycyclic aromatic hydrocarbon, and its derivatives. It is found that the conformation and molecular packing of dibenzo[a,m]rubicenes in the solid

A metal-free cycloaddition approach to highly substituted aromatic boronic esters

Moore, Jane E.,York, Mark,Harrity, Joseph P. A.

, p. 860 - 862 (2007/10/03)

Alkynylboronates participate in [4+2] benzannulation reactions to furnish highly functionalised aromatic boronic esters, further manipulation of these boronic esters has been achieved via oxidation and Suzuki coupling reactions.

One pot synthesis of 1,4-dicarboxymethyl-2,3-diphenylnaphthalene

Mallakpour, Shadpour E.

, p. 354 - 356 (2007/10/03)

Benzene 2 from aprotic diazotization of anthranilic acid 1 with isoamylnitrite and subsequent thermal decomposition of the resulted benzenediazonium-2-carboxylate (in situ), has been reacted with 2,5-dicarbomethoxy-3,4-diphenylcyclopentadienone 3 in 1,2-d

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