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Phosphorane, triethoxydifluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55422-04-3 Structure
  • Basic information

    1. Product Name: Phosphorane, triethoxydifluoro-
    2. Synonyms:
    3. CAS NO:55422-04-3
    4. Molecular Formula: C6H15F2O3P
    5. Molecular Weight: 204.154
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55422-04-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Phosphorane, triethoxydifluoro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphorane, triethoxydifluoro-(55422-04-3)
    11. EPA Substance Registry System: Phosphorane, triethoxydifluoro-(55422-04-3)
  • 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: 55422-04-3(Hazardous Substances Data)

55422-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55422-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55422-04:
(7*5)+(6*5)+(5*4)+(4*2)+(3*2)+(2*0)+(1*4)=103
103 % 10 = 3
So 55422-04-3 is a valid CAS Registry Number.

55422-04-3Downstream Products

55422-04-3Relevant articles and documents

A facile conversion of thio- and selenophosphoric acids and their derivatives into fluoridates by means of reaction with silver fluoride

Chworos, Arkadiusz,Wozniak, Lucyna A.

, p. 9337 - 9340 (1999)

Treatment of numerous thio- or selenophosphorus acids with aqueous silver fluoride in CHCl3 at room temperature results in clean formation of the corresponding fluoridates. Analogous results were obtained with other phosphorothio (seleno)ates such as esters, amidates, or halides.

Reaction of Triethyl Phosphite with Internal Perfluoroolefins and Their Aza Analogs

Rogoza,Furin

, p. 753 - 760 (2007/10/03)

Treatment of perfluoro(2-methylpent-2-ene) with triethyl phosphite gave triethoxydifluorophosphorane and diethyl perfluoro(1-ethylidene-2-methylpropenyl)phosphonate (the latter was also obtained by reaction of triethyl phosphite with perfluorotrimethylallene), while the reactions with other unsaturated perfluorinated compounds involved, together with the Arbuzov reaction, replacement of fluorine at the double bound by an ethyl group with perfluoro(1-ethylcyclohex-1-ene) and by an ethoxy group with perfluoro-(5-azanon-4-ene), perfluoro(1-azacyclohex-1-ene), and perfluoro(3-azapent-2-ene). The reactions pathways and 1H, 13C, 19F, and 31P NMR data are discussed.

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