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1-(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)-2-phenylethanone is a complex organic compound with the molecular formula C18H16O. It is a derivative of 2-phenylethanone, which is a ketone with a phenyl group attached to the 2-position of the ethanone backbone. The bicyclic structure, bicyclo[4.2.0]octa-1,3,5-trien-7-yl, adds a unique three-ring system to the molecule, with the 7-position being the point of attachment to the phenylethanone. 1-(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)-2-phenylethanone is characterized by its aromatic nature due to the presence of the phenyl group and the conjugated diene system within the bicyclic structure. It is likely to have applications in the field of organic chemistry, potentially as an intermediate in the synthesis of more complex molecules or as a compound with specific chemical properties.

6809-95-6

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6809-95-6 Usage

Chemical Structure

1-(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)-2-phenylethanone is a complex organic compound with a bicyclic ring system and a phenyl group attached to a ketone functional group.

Molecular Weight

Approximately 234.29 g/mol (calculated from the molecular formula)

Appearance

The compound is likely to be a solid, given its molecular weight and complexity.

Solubility

It is expected to be soluble in organic solvents such as ethanol, methanol, and dichloromethane due to its nonpolar nature.

Stability

The compound may be sensitive to heat, light, and moisture, as many organic compounds with multiple double bonds and aromatic rings are prone to degradation under such conditions.

Reactivity

1-(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)-2-phenylethanone can undergo various chemical reactions, such as electrophilic aromatic substitution, nucleophilic addition to the carbonyl group, and reactions involving the bicyclic ring system.

Applications

The compound is commonly used in organic synthesis and medicinal chemistry, potentially leading to the development of new pharmaceuticals or industrial materials.

Research Interest

Its unique structure and specific reactivity make it a valuable component for researchers and scientists working on the development of new compounds and materials.

Potential Uses

Due to its complex structure and reactivity, 1-(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)-2-phenylethanone may have potential pharmaceutical or industrial applications, although further research and development are required to explore these possibilities.

Check Digit Verification of cas no

The CAS Registry Mumber 6809-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,0 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6809-95:
(6*6)+(5*8)+(4*0)+(3*9)+(2*9)+(1*5)=126
126 % 10 = 6
So 6809-95-6 is a valid CAS Registry Number.

6809-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(7-bicyclo[4.2.0]octa-1,3,5-trienyl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:6809-95-6 SDS

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