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1-(4-chlorophenyl)-4,4,4-trifluoro-3-(trifluoromethyl)but-2-en-1-one is a complex chemical compound characterized by a butenone backbone with multiple fluorine atoms and a chlorophenyl group. It is known for its unique reactivity and ability to participate in various carbon-carbon bond forming reactions, making it a valuable tool in organic synthesis. Its fluorinated structure also imparts unique physical and chemical properties, which can be exploited for the development of materials and compounds with specific functionalities.

35443-99-3

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35443-99-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-chlorophenyl)-4,4,4-trifluoro-3-(trifluoromethyl)but-2-en-1-one is used as a building block for the synthesis of various organic compounds, particularly in the pharmaceutical industry. Its unique reactivity and fluorinated structure contribute to the development of new drugs with specific functionalities and improved properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(4-chlorophenyl)-4,4,4-trifluoro-3-(trifluoromethyl)but-2-en-1-one is used as a key component in the synthesis of various agrochemicals. Its complex structure and unique properties make it a promising candidate for the development of new pesticides, herbicides, and other agrochemical products with enhanced efficacy and selectivity.
Used in Organic Synthesis:
1-(4-chlorophenyl)-4,4,4-trifluoro-3-(trifluoromethyl)but-2-en-1-one is used as a valuable tool in organic synthesis due to its unique reactivity and ability to participate in various carbon-carbon bond forming reactions. This allows for the creation of a wide range of organic compounds with diverse applications in various industries.
Used in Material Science:
1-(4-chlorophenyl)-4,4,4-trifluoro-3-(trifluoromethyl)but-2-en-1-one is also of interest in material science, where its fluorinated structure can be utilized to develop materials with specific properties. These materials could have applications in various fields, such as electronics, coatings, and advanced materials for industrial use.
For further study and potential applications:
Due to its complex structure and unique properties, 1-(4-chlorophenyl)-4,4,4-trifluoro-3-(trifluoromethyl)but-2-en-1-one is of interest for further study and potential applications in various industrial and academic fields. This includes exploring its use in the development of new compounds, materials, and technologies that can benefit from its unique characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 35443-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,4 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35443-99:
(7*3)+(6*5)+(5*4)+(4*4)+(3*3)+(2*9)+(1*9)=123
123 % 10 = 3
So 35443-99-3 is a valid CAS Registry Number.

35443-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-4,4,4-trifluoro-3-(trifluoromethyl)but-2-en-1-one

1.2 Other means of identification

Product number -
Other names 4'-Chloro-4,4,4-trifluoro-3-trifluoromethylcrotonophenone

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:35443-99-3 SDS

35443-99-3Relevant academic research and scientific papers

Synthese von 4,4-Bis(trifluormethyl)-1-oxabuta-1,3-dienen

Burger, Klaus,Helmreich, Brigitte

, p. 219 - 226 (2007/10/02)

Silyl enol ethers (1) and hexafluoroacetone (2) react to give O-silylated aldol adducts 3 which, after desilylation with methanol/hydrochloric acid, are transformed into 4,4-bis(trifluoromethyl)-1-oxabuta-1,3-dienes (5) on treatment with trifluoroacetic a

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