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11,12-Dihydroindeno[2,1-a]fluorene is a polycyclic aromatic hydrocarbon (PAH) with a molecular formula of C19H14. It is a derivative of indenofluorene, which is a type of PAH consisting of a fluorene ring fused to an indene ring. 11,12-Dihydroindeno[2,1-a]fluorene is characterized by its unique structure, where the fluorene ring is partially hydrogenated, resulting in a dihydro derivative. 11,12-Dihydroindeno[2,1-a]fluorene is of interest in chemical research due to its potential applications in materials science and as a precursor in the synthesis of other complex organic compounds. It is also studied for its environmental and health implications, as some PAHs are known to be carcinogenic. The compound is typically synthesized through various chemical reactions and can be found in trace amounts in certain environmental samples, such as coal tar and petroleum products.

5815-59-8

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5815-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5815-59-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5815-59:
(6*5)+(5*8)+(4*1)+(3*5)+(2*5)+(1*9)=108
108 % 10 = 8
So 5815-59-8 is a valid CAS Registry Number.

5815-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 11,12-dihydro-indeno[2,1-a]fluorene

1.2 Other means of identification

Product number -
Other names 11,12-Dihydro-indeno[2,1-a]fluoren

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:5815-59-8 SDS

5815-59-8Relevant academic research and scientific papers

Gold(I) carbenes by retro-buchner reaction: Generation and fate

Wang, Yahui,McGonigal, Paul R.,Herle, Bart,Besora, Maria,Echavarren, Antonio M.

supporting information, p. 801 - 809 (2014/02/14)

The fate of the aryl gold(I) carbenes generated by retro-Buchner reaction of ortho-substituted 7-aryl-1,3,5-cycloheptatrienes is dependent on the constitution of the ortho substituent. Indenes and fluorenes are obtained by intramolecular reaction of highly electrophilic gold(I) carbenes with alkenes and arenes. According to density functional theory calculations, the gold-catalyzed retro-Buchner process occurs stepwise, although the two carbon-carbon cleavages occur on a rather flat potential energy surface.

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