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3,6-dimethyl-9H-fluorene is an organic compound with the molecular formula C15H14. It is a derivative of fluorene, a polycyclic aromatic hydrocarbon, characterized by the presence of two methyl groups attached to the 3rd and 6th carbon atoms of the fluorene core. 3,6-dimethyl-9H-fluorene is known for its unique chemical structure, which contributes to its distinct properties and potential applications in various fields, such as organic synthesis and materials science. Due to its aromatic nature, 3,6-dimethyl-9H-fluorene exhibits stability and can be used as a building block for more complex molecules. It is also of interest in the study of the physical and chemical properties of polycyclic aromatic hydrocarbons, which are relevant to areas such as environmental chemistry and pharmaceuticals.

7495-37-6

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7495-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7495-37-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7495-37:
(6*7)+(5*4)+(4*9)+(3*5)+(2*3)+(1*7)=126
126 % 10 = 6
So 7495-37-6 is a valid CAS Registry Number.

7495-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dimethyl-9H-fluorene

1.2 Other means of identification

Product number -
Other names 3,6-dimethyl-fluorene

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

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More Details:7495-37-6 SDS

7495-37-6Downstream Products

7495-37-6Relevant academic research and scientific papers

Dications of fluorenylidenes. The effect of substituent electronegativity and position on the antiaromaticity of substituted tetrabenzo[5.5]fulvalene dications

Levy, Amalia,Rakowitz, Amber,Mills, Nancy S.

, p. 3990 - 3998 (2007/10/03)

Oxidation of 3,6-disubstituted tetrabenzo[5.5]fulvalenes by SbF5 results in the formation of dications that behave like two antiaromatic fluorenyl cations connected by a single bond. Both fluorenyl systems exhibit the paratropic shifts and nucleus independent chemical shifts (NICS) characteristic of antiaromatic species. Comparison with analogous 2,7-disubstituted tetrabenzo[5.5]fulvalenes reveals that the antiaromaticity of the substituted ring system can be altered substantially by changes in the placement of the substituents, possibly due to changes in the delocalization of charge in the system. Substituents in the 3,6-position decrease the antiaromaticity because of the increase in the benzylic resonance compared to 2,7-substituents.

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