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3300-10-5

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3300-10-5 Usage

General Description

Ethanone, 1-(9H-fluoren-9-yl)- is a chemical compound with a molecular formula of C15H12O. It is a ketone that contains a fluorene group, which is a polycyclic aromatic hydrocarbon. Ethanone, 1-(9H-fluoren-9-yl)- is commonly used in organic synthesis as a building block for creating various molecules due to its unique structure and reactivity. It can also be utilized as a fluorescent marker or dye in research and laboratory applications. Ethanone, 1-(9H-fluoren-9-yl)- may have potential uses in pharmaceuticals, materials science, and other industries for its distinctive properties.

Check Digit Verification of cas no

The CAS Registry Mumber 3300-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3300-10:
(6*3)+(5*3)+(4*0)+(3*0)+(2*1)+(1*0)=35
35 % 10 = 5
So 3300-10-5 is a valid CAS Registry Number.

3300-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(9H-fluoren-9-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-fluoren-9-yl-ethanone

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:3300-10-5 SDS

3300-10-5Relevant articles and documents

Acid-catalyzed Reactions of 1,2-Dicarbonylethanes with Benzene. Ethylene Dication Electrophiles.

Yamazaki, Takahisa,Saito, Shin-ichi,Ohwada, Tomohiko,Shudo, Koichi

, p. 5749 - 5752 (1995)

1,2-dicarbonyl compounds reacted with benzene in the presence of a strong acid, trifluoromethanesulfonic acid, to give gem-diphenylated ketones in high yields.The reaction was accelerated when the acidity of the medium was increased, supporting involvement of O,O-diprotonated 1,2-dicarbonyl species (i.e., 1,2-dihydroxyethylene dications) as the active electrophiles.

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