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2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE is a fluorinated compound characterized by a perfluorinated alkyl chain and a tetrafluoroethanesulfonyl fluoride group. It is recognized for its high thermal and chemical stability, which makes it suitable for a variety of industrial applications.

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  • 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE

    Cas No: 73606-15-2

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  • 2-(8-chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-hexadecafluorooctoxy)-1,1,2,2-tetrafluoroethanesulfonyl fluoride

    Cas No: 73606-15-2

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  • 73606-15-2 Structure
  • Basic information

    1. Product Name: 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE
    2. Synonyms: 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE;ETHANESULFONYL FLUORIDE, 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUORO-;2-[(8-chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-hexadecafluorooctyl)oxy]-;2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE
    3. CAS NO:73606-15-2
    4. Molecular Formula: C10ClF21O3S
    5. Molecular Weight: 634.59
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73606-15-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 261.0±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.827±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Hygroscopic, Refrigerator, under inert atmosphere
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE(73606-15-2)
    11. EPA Substance Registry System: 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE(73606-15-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 73606-15-2(Hazardous Substances Data)

73606-15-2 Usage

Uses

Used in the Production of Fluorinated Polymers:
2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE is used as a precursor for the synthesis of perfluoroalkylated compounds, which are essential in the production of fluorinated polymers. These polymers are valued for their exceptional durability and resistance to extreme conditions.
Used in the Creation of Surfactants:
In the surfactant industry, this compound serves as a crucial building block for the development of surfactants that exhibit unique properties, such as high stability and resistance to various environmental factors.
Used in Pharmaceutical Synthesis:
2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE is utilized as a starting material in the synthesis of pharmaceuticals, where its unique properties can contribute to the development of novel drugs with enhanced efficacy and stability.
Used in Specialty Materials:
2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE is also used as a building block in the synthesis of specialty materials that possess unique properties, such as low surface energy and high hydrophobicity, which are desirable in various high-performance applications.
Used in Water and Oil Repellent Coatings:
Due to its fluorinated nature, 2-[(8-CHLORO-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-HEXADECAFLUOROOCTYL)OXY]-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE exhibits low surface energy and high hydrophobicity, making it valuable in the development of coatings that repel water and oil, thus finding applications in various industries where non-stick and easy-to-clean surfaces are required.

Check Digit Verification of cas no

The CAS Registry Mumber 73606-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,0 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73606-15:
(7*7)+(6*3)+(5*6)+(4*0)+(3*6)+(2*1)+(1*5)=122
122 % 10 = 2
So 73606-15-2 is a valid CAS Registry Number.

73606-15-2SDS

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 2-(8-chloro-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-hexadecafluorooctoxy)-1,1,2,2-tetrafluoroethanesulfonyl fluoride

1.2 Other means of identification

Product number -
Other names 2-{2-[2-(2-aminophenoxy)ethoxy]ethoxy}phenylamine

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:73606-15-2 SDS

73606-15-2Downstream Products

73606-15-2Relevant articles and documents

Redox-Initiated Per(poly)fluoroalkylation of Olefins by Per(poly)fluoroalkyl Chlorides

Hu, Chang-Ming,Qing, Feng-Ling

, p. 6348 - 6351 (2007/10/02)

The per(poly)fluoroalkylation of olefins by per(poly)fluoroalkyl chlorides, initiated by ammonium persulfate/sodium formate ((NH4)2S2O8/HCO2Na), is described.The reaction proceeds smoothly in polar aprotic solvents. The presence of functional groups like sodium carboxylate or sulfonate in the polyfluoroalkyl chloride appear to facilitate the reaction.The reaction appears to be initiated by a single-electron transfer, represents the firat example of the reactivity of per(poly)fluoroalkyl chlorides, and also demonstrates their use as per(poly)fluoroalkylating agents.For α-chloro-ω-iodoperfluoroalkanes only the carbon-iodine bond is cleaved during the reaction.An explantation for the apparent stability of the carbon-chlorine bond in such compounds is given.

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