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Lithium, (2,5-difluorophenyl)is a chemical compound that belongs to the class of organolithium reagents, which are commonly used in organic synthesis. It is a highly reactive compound that can easily undergo reactions with other organic molecules, making it a valuable tool in the development of new chemical compounds. Lithium, (2,5-difluorophenyl)is also studied for its potential applications in lithium-ion battery technologies and as a catalyst in organic reactions. Due to its reactivity and potential hazards, it is important to handle Lithium, (2,5-difluorophenyl)- with caution.

25152-36-7

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25152-36-7 Usage

Uses

Used in Organic Synthesis:
Lithium, (2,5-difluorophenyl)is used as a reagent in the preparation of various organic compounds, including pharmaceuticals, agrochemicals, and advanced materials. Its high reactivity allows it to readily participate in reactions with other organic molecules, facilitating the synthesis of complex organic structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Lithium, (2,5-difluorophenyl)is used as a key intermediate in the synthesis of various drug molecules. Its unique reactivity enables the formation of specific chemical bonds that are crucial for the development of new pharmaceutical agents.
Used in Agrochemical Industry:
Lithium, (2,5-difluorophenyl)is also utilized in the agrochemical industry for the synthesis of various agrochemicals, such as pesticides and herbicides. Its ability to form specific chemical bonds contributes to the development of effective and targeted agrochemical products.
Used in Advanced Materials:
In the field of advanced materials, Lithium, (2,5-difluorophenyl)is used as a precursor in the synthesis of novel materials with unique properties. Its reactivity allows for the creation of materials with tailored characteristics for specific applications, such as high-performance polymers and functional materials.
Used in Lithium-ion Battery Technologies:
Lithium, (2,5-difluorophenyl)has been studied for its potential applications in lithium-ion battery technologies. Its unique chemical properties may contribute to the development of improved battery systems with enhanced performance and energy density.
Used as a Catalyst in Organic Reactions:
In addition to its use as a reagent, Lithium, (2,5-difluorophenyl)can also function as a catalyst in various organic reactions. Its ability to facilitate specific chemical transformations can improve the efficiency and selectivity of these reactions, leading to the production of desired products with higher yields and purity.

Check Digit Verification of cas no

The CAS Registry Mumber 25152-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,5 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25152-36:
(7*2)+(6*5)+(5*1)+(4*5)+(3*2)+(2*3)+(1*6)=87
87 % 10 = 7
So 25152-36-7 is a valid CAS Registry Number.

25152-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name lithium,1,4-difluorobenzene-6-ide

1.2 Other means of identification

Product number -
Other names 1,4-difluorobenzene-6-ide

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:25152-36-7 SDS

25152-36-7Upstream product

25152-36-7Downstream Products

25152-36-7Relevant academic research and scientific papers

Lithium diisopropylamide-mediated ortholithiations: Lithium chloride catalysis

Gupta, Lekha,Hoepker, Alexander C.,Singh, Kanwal J.,Collum, David B.

supporting information; experimental part, p. 2231 - 2233 (2009/08/07)

Ortholithiations of a range of arenes mediated by lithium diisopropylamide (LDA) in THF at -78 °C reveal substantial accelerations by as little as 0.5 mol % of LiCl (relative to LDA). Substrate dependencies suggest a specific range of reactivity within wh

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