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1-Phenyl-3-[3-(trifluoromethyl)phenyl]acetone is a specialty chemical compound with significant importance in organic chemistry. It is characterized by its molecular formula C16H14F3O and belongs to the chemical class of fluoroalkyls and fluoroarylalkyls. 1-Phenyl-3-[3-(trifluoromethyl)phenyl]acetone features a trifluoromethyl group, phenyl rings, and a ketone group, which suggests that it possesses the properties of both a trifluoromethyl compound and a ketone. Trifluoromethyl compounds are known for their potent chemical and biological activities, making them valuable in various applications, particularly in the pharmaceutical industry. While specific details of its applications may be proprietary or not publicly disclosed, it is likely used extensively in research and development settings.

59756-57-9

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59756-57-9 Usage

Uses

Used in Pharmaceutical Industry:
1-Phenyl-3-[3-(trifluoromethyl)phenyl]acetone is used as a key intermediate in the synthesis of various pharmaceutical compounds for its unique chemical properties. The presence of the trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting drugs, potentially leading to improved pharmacokinetics and therapeutic efficacy.
Used in Organic Synthesis:
In the field of organic synthesis, 1-Phenyl-3-[3-(trifluoromethyl)phenyl]acetone serves as a versatile building block for the creation of a wide range of organic molecules. Its reactivity and functional groups make it suitable for various synthetic transformations, such as condensation, reduction, and oxidation reactions, enabling the development of novel chemical entities with potential applications in various industries.
Used in Research and Development:
1-Phenyl-3-[3-(trifluoromethyl)phenyl]acetone is utilized in research and development settings to explore its potential applications and properties. Scientists and chemists investigate its reactivity, stability, and interactions with other molecules to gain insights into its behavior and possible uses in various chemical processes and applications.
While the specific applications of 1-Phenyl-3-[3-(trifluoromethyl)phenyl]acetone in manufacturing, science, or medicine may not be publicly available, its unique properties and potential as a trifluoromethyl compound make it a valuable asset in the fields of pharmaceuticals, organic synthesis, and research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 59756-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,5 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59756-57:
(7*5)+(6*9)+(5*7)+(4*5)+(3*6)+(2*5)+(1*7)=179
179 % 10 = 9
So 59756-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H13F3O/c17-16(18,19)14-8-4-7-13(9-14)11-15(20)10-12-5-2-1-3-6-12/h1-9H,10-11H2

59756-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-[3-(trifluoromethyl)phenyl]propan-2-one

1.2 Other means of identification

Product number -
Other names EINECS 261-915-0

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:59756-57-9 SDS

59756-57-9Relevant academic research and scientific papers

Synthesis method of 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone

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, (2021/11/21)

The invention belongs to the technical field of chemical intermediates, and particularly relates to a synthesis method of 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone. A compound A is used as a basic raw material, and 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone is obtained through Blanc chloromethylation, substitution reaction, Claisen ester condensation and hydrolysis reaction in sequence. The synthesis method of 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone is high in purity, high in yield and simple to operate.

Synthesis of phenylacetic acid esters

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, (2008/06/13)

Esters of phenylacetic acids are prepared in a single step by hydrolysis of 2,2,2-trichloro-1-phenylethanes in inorganic basic media.

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