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2,3,4,5-Tetramethylbicyclo[4.2.0]octa-1,3,5-trien-7-one is a complex organic compound with the molecular formula C13H16O. It is a bicyclic aromatic ketone, characterized by its unique structure with four methyl groups attached to the bicyclic ring system. 2,3,4,5-Tetramethylbicyclo[4.2.0]octa-1,3,5-trien-7-one is known for its potential applications in the synthesis of various organic molecules and pharmaceuticals due to its reactive nature and structural diversity. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its reactivity and stability, make it a valuable building block in organic chemistry, although its specific applications and safety considerations should be carefully evaluated.

6590-36-9

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6590-36-9 Usage

Bicyclic Compound

2,3,4,5-Tetramethylbicyclo[4.2.0]octa-1,3,5-trien-7-one is a chemical compound that belongs to the class of bicyclic compounds, characterized by its two inter-connected carbon rings.

Synthetic Aroma Compound

It is primarily used in the fragrance and flavor industry as a synthetic aroma compound, commonly used as a fragrance ingredient to create a woody, earthy, and mossy aroma.

Application in Perfumes and Scented Products

It is used in the production of perfumes, colognes, and other scented products.

Potential Medicinal Applications

Isodurene has been studied for its potential applications in medicinal and pharmaceutical industries due to its unique chemical properties.

Also known as Isodurene

It is also known by the name isodurene.

Check Digit Verification of cas no

The CAS Registry Mumber 6590-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6590-36:
(6*6)+(5*5)+(4*9)+(3*0)+(2*3)+(1*6)=109
109 % 10 = 9
So 6590-36-9 is a valid CAS Registry Number.

6590-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5-tetramethylbicyclo[4.2.0]octa-1,3,5-trien-7-one

1.2 Other means of identification

Product number -
Other names 2,3,4,5-Tetramethyl-bicyclo[4,2,0]octa-1,3,5-trien-7-on

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:6590-36-9 SDS

6590-36-9Relevant academic research and scientific papers

THERMAL ADDITION REACTIONS TO BENZOCYCLOBUTENONES STUDIED BY FLASH PHOTOLYSIS

Schiess, P.,Eberle, M.,Huys-Francotte, M.,Wirz, J.

, p. 2201 - 2204 (2007/10/02)

Ortho-quinoid vinylketenes 2 have been generated thruogh flash photolysis of benzocyclobutenones 1.A kinetic study of intermolecular addition reactions of 2 competing with the recyclization 2 -> 1 reveals strikingly different substituent effects for the addition of methanol and of dienophiles.

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