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HEXAFLUOROISOPROPYL 2-FLUOROACRYLATE, with the molecular formula C6H3F7O2, is a colorless liquid characterized by a pungent odor. This chemical compound serves as a versatile monomer in the synthesis of polymers and copolymers, which are utilized across a spectrum of industries for their unique properties.

74359-06-1

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74359-06-1 Usage

Uses

Used in Polymer and Copolymer Production:
HEXAFLUOROISOPROPYL 2-FLUOROACRYLATE is used as a monomer for the production of polymers and copolymers, which are valued for their specific characteristics in various applications. The reason for its use in this capacity is due to its ability to contribute to the formation of materials with tailored properties, such as enhanced durability, chemical resistance, and thermal stability.
Used in Coatings Industry:
In the coatings industry, HEXAFLUOROISOPROPYL 2-FLUOROACRYLATE is used as a component in the formulation of high-performance coatings. These coatings benefit from the compound's properties, which may include resistance to environmental factors, such as UV radiation, moisture, and chemical exposure, thereby extending the service life of the coated surfaces.
Used in Adhesives Industry:
HEXAFLUOROISOPROPYL 2-FLUOROACRYLATE is also utilized as a component in adhesive formulations, where it enhances the adhesive's bonding strength and resistance to various conditions. This makes the adhesives suitable for a wide range of applications, including industrial assembly, automotive, and construction sectors.
Used in Specialty Materials Industry:
HEXAFLUOROISOPROPYL 2-FLUOROACRYLATE serves as a building block in the synthesis of specialty materials, which are designed for specific high-performance applications. These materials may be used in sectors such as aerospace, electronics, and medical devices, where unique combinations of properties, such as biocompatibility, electrical insulation, or mechanical strength, are required.
Used in Specialty Chemicals and Pharmaceuticals:
HEXAFLUOROISOPROPYL 2-FLUOROACRYLATE is used as a starting material in the synthesis of specialty chemicals and pharmaceuticals, where its unique structure can be leveraged to create new compounds with specific therapeutic effects or other desired properties.
Safety Considerations:
Given that HEXAFLUOROISOPROPYL 2-FLUOROACRYLATE is classified as a hazardous chemical, it is crucial to handle it with care in a controlled environment. This precaution is taken to minimize exposure and prevent potential health risks to individuals working with the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 74359-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74359-06:
(7*7)+(6*4)+(5*3)+(4*5)+(3*9)+(2*0)+(1*6)=141
141 % 10 = 1
So 74359-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F7O2/c1-2(7)3(14)15-4(5(8,9)10)6(11,12)13/h4H,1H2

74359-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,3,3-hexafluoropropan-2-yl 2-fluoroprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-fluoro-2-propenoic acid 1,1,1,2,3,3-hexafluoropropan-2-yl ester

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:74359-06-1 SDS

74359-06-1Downstream Products

74359-06-1Relevant articles and documents

Process for the synthesis of fluoroorganic compounds

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, (2008/06/13)

The present invention relates to a fluorination method for the synthesis of halofluoroorganic compounds which can be used, inter alia, as precursors in the synthesis of 2,3-unsaturated fluoroorganic carbonyl compounds comprising a fluorine substituent in the 2 position.

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