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Pentanenitrile, 2,2-difluoro-4,4-dimethyl-3-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 219866-68-9 Structure
  • Basic information

    1. Product Name: Pentanenitrile, 2,2-difluoro-4,4-dimethyl-3-oxo-
    2. Synonyms: Pentanenitrile, 2,2-difluoro-4,4-dimethyl-3-oxo-
    3. CAS NO:219866-68-9
    4. Molecular Formula: C7H9F2NO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219866-68-9.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: Pentanenitrile, 2,2-difluoro-4,4-dimethyl-3-oxo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pentanenitrile, 2,2-difluoro-4,4-dimethyl-3-oxo-(219866-68-9)
    11. EPA Substance Registry System: Pentanenitrile, 2,2-difluoro-4,4-dimethyl-3-oxo-(219866-68-9)
  • 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: 219866-68-9(Hazardous Substances Data)

219866-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219866-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,8,6 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 219866-68:
(8*2)+(7*1)+(6*9)+(5*8)+(4*6)+(3*6)+(2*6)+(1*8)=179
179 % 10 = 9
So 219866-68-9 is a valid CAS Registry Number.

219866-68-9Upstream product

219866-68-9Downstream Products

219866-68-9Relevant articles and documents

Catalyzed fluorination of carbonyl compounds

-

, (2008/06/13)

The present invention provides a method of substituting a carbonyl compound with fluorine at the α-position, comprising reaching the carbonyl compound with a fluorinating present of a metal-containing catalyst. The reaction results in replacement of a hydrogen atom by fluorine. The catalyst, which is used in a catalytically effective amount, is preferably a transition metal. In one class of methods the catalyst is a transition metal compound. In another class of methods, the catalyst is an elemental metal, in which case the carbonyl compound has an activating group attached to the carbon atom which is substituted by fluorine.

Elemental fluorine. Part 9 : Catalysis of the direct fluorination of 2-substituted carbonyl compounds

Chambers, Richard D.,Hutchinson, John

, p. 45 - 52 (2007/10/03)

Catalysis of the reaction between fluorine and a range of 2-substituted carbonyl compounds has been investigated. Most notably, the preparation of diethyl-2-fluoromalonate has been achieved in high yield by fluorination of diethylmalonate in the presence of hydrated copper nitrate. Reactions between fluorine and carbanions derived from 2-substituted carbonyl compounds, including phosphonates, sulphones and nitriles, are also discussed.

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