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1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE

    Cas No: 144951-88-2

  • USD $ 1.9-2.9 / Gram

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  • 144951-88-2 Structure
  • Basic information

    1. Product Name: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE
    2. Synonyms: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE
    3. CAS NO:144951-88-2
    4. Molecular Formula: C4HF8N3O3S
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144951-88-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE(144951-88-2)
    11. EPA Substance Registry System: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE(144951-88-2)
  • 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: 144951-88-2(Hazardous Substances Data)

144951-88-2 Usage

Class

Sulfonamide derivative

Use

Reagent in organic synthesis

Application fields

Fluorine chemistry, pharmaceutical research

Function

Introduces fluorine atoms into organic molecules

Property

Enhances chemical and biological properties of molecules

Structure

Unique and reactive

Importance

Valuable tool in developing new materials and pharmaceuticals

Hazard

Potentially explosive substance

Safety

Requires careful handling

Check Digit Verification of cas no

The CAS Registry Mumber 144951-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,9,5 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144951-88:
(8*1)+(7*4)+(6*4)+(5*9)+(4*5)+(3*1)+(2*8)+(1*8)=152
152 % 10 = 2
So 144951-88-2 is a valid CAS Registry Number.

144951-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-diazo-1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)ethanesulfonamide

1.2 Other means of identification

Product number -
Other names -

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:144951-88-2 SDS

144951-88-2Relevant articles and documents

Facile and quantitative synthesis of 1,3-diazaheterocycle-fused 1,2,3-triazole derivatives using fluoroalkanesulfonyl azide as a diazo transfer reagent

Gu, Jiwei,Xiong, Wanting,Zhang, Zhenhua,Zhu, Shizheng

body text, p. 1717 - 1722 (2011/07/29)

A series of 1,3-diazaheterocycle-fused 1,2,3-triazoles were conveniently and quantitatively prepared by 1,3-dipolar cycloaddition of heterocyclic ketene aminals with fluoroalkanesulfonyl azide, followed by elimination of fluoroalkanesulfonyl amide at room

Synthesis and Reactions of Fluoroalkanesulfonyl Azides and N,N-Dichlorofluoroalkanessulfonamides

Zhu, Shi-Zheng

, p. 2077 - 2082 (2007/10/02)

Thermolysis or photolysis of fluoroalkanesulfonyl azides RFSO2N3 afforded the corresponding nitrene intermediates RFSo2N which reacted readily with alkanes, alkenes, benzene, dimethyl sulfide, dimethyl sulfoxide, pyridine and triphenylphosphine to give insertion or addition products.Similar results were obtained by the reactions of N,N-dichlorofluoroalkanesulfonamides, RFSO2NCl2, with the same reagents in the presence of zinc powder.Treatment of RFSO2NCl2 with alkene in the absence of zinc powder gave only a 1:1 adduct via a free-radical intermediate RfSO2NCl.

Synthesis of fluoroalkanesulfonyl azides and their reactions as fluoroalkanesulfonyl nitrene precursors

Zhu, Shi-Zheng

, p. 6503 - 6504 (2007/10/02)

Thermolysis or photolysis of the title compounds with cyclohexane, Me2C = CMe2, methyl sulfide and triphenyl phosphine gave the corresponding insertion or addition products via the perfluoroalkanesulfonyl nitrene intermediate.

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