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Ethanone, 2-fluoro-1-(3-methylphenyl)(9CI), also known as 2-fluoro-1-(3-methylphenyl)ethanone, is a chemical compound belonging to the ketone class. It possesses a molecular formula of C9H9FO and a molecular weight of 152.165 g/mol. Identified by its CAS number 55303-67-4, Ethanone, 2-fluoro-1-(3-methylphenyl)- (9CI) is characterized by the presence of a fluorine atom and a methyl group attached to a phenyl ring, which endows it with unique chemical properties and reactivity.

2560-97-6

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2560-97-6 Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 2-fluoro-1-(3-methylphenyl)(9CI) is utilized as a building block in the synthesis of pharmaceuticals due to its unique structure and reactivity. Its fluorinated ketone nature allows for the introduction of additional functional groups, making it a versatile intermediate for the development of new drugs with tailored properties for specific therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Ethanone, 2-fluoro-1-(3-methylphenyl)(9CI) serves as a key intermediate in the production of various agrochemicals. Its specific properties enable the synthesis of compounds with potential applications in pest control, crop protection, and other agricultural practices, contributing to the development of more effective and targeted agrochemical products.
Used in Medicinal Chemistry Research:
Ethanone, 2-fluoro-1-(3-methylphenyl)(9CI) is employed in medicinal chemistry research for the exploration of its potential applications in drug discovery. Its unique structure and reactivity make it a valuable compound for studying the effects of fluorination and other modifications on the biological activity of molecules, aiding in the design of novel therapeutic agents.
Used in Material Science:
In the field of material science, Ethanone, 2-fluoro-1-(3-methylphenyl)(9CI) has potential applications in the development of new materials with specific properties. Its fluorinated ketone structure can be exploited to create materials with tailored characteristics, such as improved stability, reactivity, or selectivity, for use in various industrial processes or applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2560-97-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2560-97:
(6*2)+(5*5)+(4*6)+(3*0)+(2*9)+(1*7)=86
86 % 10 = 6
So 2560-97-6 is a valid CAS Registry Number.

2560-97-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-1-(3-methylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-fluoro-1-(m-tolyl)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:2560-97-6 SDS

2560-97-6Downstream Products

2560-97-6Relevant academic research and scientific papers

Synthesis of α-Fluoroketones from Vinyl Azides and Mechanism Interrogation

Wu, Shu-Wei,Liu, Feng

supporting information, p. 3642 - 3645 (2016/08/16)

An efficient and mild fluorination of vinyl azides for the synthesis of α-fluoroketones is described. The mechanistic studies indicated that a single-electron transfer (SET) and a subsequent fluorine atom transfer process could be involved in the reaction.

Metal-free, efficient oxyfluorination of olefins for the synthesis of α-fluoroketones

Yang, Qiang,Mao, Liu-Liang,Yang, Bin,Yang, Shang-Dong

supporting information, p. 3460 - 3463 (2014/07/21)

A novel oxyfluorination of olefin reactions has been developed. The reactions involve a metal-free and green catalytic system for the synthesis of α-fluoroketones which is an important building block for organic synthesis. Moreover, this reaction system exhibits great functional group tolerance.

One-pot α-nucleophilic fluorination of acetophenones in a deep eutectic solvent

Chen, Zizhan,Zhu, Wei,Zheng, Zubiao,Zou, Xinzhuo

experimental part, p. 340 - 344 (2010/06/11)

Two methods of nucleophilic fluorination to prepare α-fluoroacetophenones from α-bromoacetophenones by using KF with PEG-400 or TBAF with ZnF2 are described. On the fundamental of nucleophilic fluorination, a novel method of one-pot fluorination to prepare α-fluoroacetophenones directly from acetophenones in DES was developed.

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