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Ethanone, 1-[2-(dimethylamino)phenyl](9CI) is a chemical compound characterized by the molecular formula C11H15NO. It is a ketone derivative featuring a phenyl group with a dimethylamino substituent, which endows it with unique structural and reactivity properties. Ethanone, 1-[2-(dimethylamino)phenyl](9CI) is of interest in the realms of organic synthesis and pharmaceutical research, and it may serve as a precursor for the development of biologically active molecules in medicinal chemistry.

10336-55-7

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10336-55-7 Usage

Uses

Used in Organic Synthesis:
Ethanone, 1-[2-(dimethylamino)phenyl](9CI) is utilized as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Ethanone, 1-[2-(dimethylamino)phenyl](9CI) is employed as a building block for the synthesis of biologically active compounds. Its presence in the molecular structure can influence the pharmacological properties of the final product, such as potency, selectivity, and bioavailability. Researchers leverage its reactivity to create novel drug candidates with potential therapeutic applications.
Used in Medicinal Chemistry:
Ethanone, 1-[2-(dimethylamino)phenyl](9CI) holds promise in medicinal chemistry for its potential to be incorporated into the design of new pharmaceutical agents. Its structural features can be exploited to enhance the drug-like properties of molecules, such as improving their solubility, stability, and interaction with biological targets. Further studies are necessary to explore its full potential in the discovery and development of innovative therapeutics.
While the provided materials do not specify particular applications or industries for Ethanone, 1-[2-(dimethylamino)phenyl](9CI), the general uses outlined above are based on its role in organic synthesis, pharmaceutical research, and medicinal chemistry. Further exploration and research are required to identify specific applications and industries where Ethanone, 1-[2-(dimethylamino)phenyl]- (9CI) can be effectively utilized.

Check Digit Verification of cas no

The CAS Registry Mumber 10336-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,3 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10336-55:
(7*1)+(6*0)+(5*3)+(4*3)+(3*6)+(2*5)+(1*5)=67
67 % 10 = 7
So 10336-55-7 is a valid CAS Registry Number.

10336-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,N-dimethylaminoacetophenone

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:10336-55-7 SDS

10336-55-7Relevant academic research and scientific papers

Versatile synthesis of novel tetrahydroquinolines as potentially active semicarbazide-sensitive amine oxidase (SSAO) inhibitors via tert-Amino effect

Deme, Ruth,Schlich, Michele,Mucsi, Zoltán,Karvaly, Gellért,Tóth, Gergo,Mátyus, Péter

, p. 164 - 196 (2016/10/22)

Several aminomethyl tetrahydroquinoline derivatives were synthesized in a facile three-ste procedure, in order to develop a semicarbazide-sensitive amine oxidase (SSAO) inhibitor library as proved by in vitro test on rat aorta microsomal fraction. The eff

Efficient and recyclable rare earth-based catalysts for Friedel-Crafts acylations under microwave heating: Dendrimers show the way

Perrier, Arnaud,Keller, Michel,Caminade, Anne-Marie,Majoral, Jean-Pierre,Ouali, Armelle

supporting information, p. 2075 - 2080 (2013/09/24)

The catalytic system involving Sc(OTf)3 and a dendritic terpyridine ligand is able to promote the Friedel-Crafts acylation of a wide range of aromatics under microwave irradiation. The expected products are obtained in high yields after short reaction times and the nano-sized catalyst can be recovered and successfully used in 12 consecutive runs.

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