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1-(9,9-DiMethyl-9H-fluoren-2-yl)ethanone, also known as 1-(9,9-dimethylfluoren-2-yl)ethanone, is a chemical compound that belongs to the ketone class. It is a yellow crystalline solid with unique physical and chemical properties due to the presence of a fluorene group in its structure. 1-(9,9-DiMethyl-9H-fluoren-2-yl)ethanone is commonly used in organic synthesis and serves as a building block for the preparation of various pharmaceuticals and agrochemicals.

72322-75-9

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72322-75-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(9,9-DiMethyl-9H-fluoren-2-yl)ethanone is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds with different therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(9,9-DiMethyl-9H-fluoren-2-yl)ethanone is used as a starting material for the development of new agrochemicals, such as pesticides and herbicides, that can help improve crop yield and protect plants from pests.
Used in Chemical Research:
1-(9,9-DiMethyl-9H-fluoren-2-yl)ethanone is utilized as a reagent in chemical research, where it aids in the synthesis and analysis of various organic compounds.
Used in Dyes and Pigments Manufacturing:
1-(9,9-DiMethyl-9H-fluoren-2-yl)ethanone is also used in the manufacturing of dyes and pigments, where its unique properties contribute to the development of new colorants with improved characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 72322-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,2 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72322-75:
(7*7)+(6*2)+(5*3)+(4*2)+(3*2)+(2*7)+(1*5)=109
109 % 10 = 9
So 72322-75-9 is a valid CAS Registry Number.

72322-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(9,9-dimethylfluoren-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-(9,9-dimethyl-9H-fluoren-2-yl)

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:72322-75-9 SDS

72322-75-9Relevant academic research and scientific papers

Facile synthesis and characterization of indene-fused 4-methylcoumarins and an unexpected skeletal rearrangement via Pechmann condensation

Wu, Jie,Liu, Wei,Liang, Li,Gan, Ya,Xia, Shuang,Gou, Xiaojun,Sun, Xiaohua

supporting information, (2020/04/15)

The Pechmann condensation of phenolic fluorenes with ethyl acetoacetate afforded indene-fused 4-methylcoumarins. In addition to the expected indeno[1,2-g]coumarin, a skeletal rearranged compound was obtained as a concomitant product when 9,9-dimethyl-9H-fluorene-2,7-diol was utilized as the substrate. X-ray crystallography was used to identify the structures of the isomers. Photochemical and photophysical studies indicated that compared with the non-rearranged products, the skeletal rearranged isomers have red shifted absorption maxima and much higher fluorescence quantum yields. A mechanism involving two competitive pathways for the simultaneous production of isomers was proposed.

Efficient luminescence from fluorene- and spirobifluorene-based lanthanide complexes upon near-visible irradiation

Bottaro, Gregorio,Rizzo, Fabio,Cavazzini, Marco,Armelao, Lidia,Quici, Silvio

supporting information, p. 4598 - 4607 (2014/05/06)

We describe herein the synthesis and photophysical characterization of new lanthanide complexes that consist of a (9,9-dimethylfluoren-2-yl)-2-oxoethyl or a (9,9-spirobifluoren-2-yl)-2-oxoethyl unit as the antenna, covalently linked to a 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (DO3A) unit as the Ln3+ (Gd3+, Eu3+, Sm3+, Tb 3+, Dy3+) coordination site. We were able to translate the spectroscopic properties of the innovative bipartite ligands into the formation of highly luminescent europium complexes that exhibit efficient emission (φse>0.1) upon sensitization in the near-visible region, that is, with an excitation wavelength above 350 nm. The luminescence of the Eu 3+complexes is clearly detectable at concentrations as low as 10 pM. Furthermore, the structural organization of these bipartite ligands makes the complexes highly soluble in aqueous solutions and chemically stable over time. Lighting up: Innovative fluorene- and spirobifluorene-based lanthanide complexes show efficient luminescence upon sensitization in the near-visible region. Lanthanide emission is detectable at concentration as low as 10 pM in aqueous solution (see figure).

Synthesis and properties of alkynethiolate gold(i) complexes

Lardies, Nora,Romeo, Inocencio,Cerrada, Elena,Laguna, Mariano,Skabara, Peter J.

, p. 5329 - 5338 (2008/03/18)

A series of alkynethiolate gold(i) derivatives have been synthesised by the cleavage of 4-monosubstituted 1,2,3-thiadiazoles in the presence of strong bases. The syntheses of the 1,2,3-thiadiazoles with p-cyanophenyl, p-tolyl, 2-thienyl, 3-thienyl and 9,9-dimethylfluoren-2-yl fragments are also described. All the complexes have been characterised by spectroscopic techniques and the complexes [Au(p-CH3-C6H4-CC-S)PPh3], [Au(3-C4H3S-CC-S)PPh3] and PPN[Au(p-CH 3-C6H4-CC-S)(C6F5)] by X-ray analysis. The electrochemically polymerizable mononuclear bis(alkynethiolate) gold(i) complex PPN[Au(3-C4H3S-CC-S) 2] is also described, including its electropolymerization and electrochemical properties. This journal is The Royal Society of Chemistry.

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