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5-[2-(2-chloroethyl)phenyl]dihydrofuran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 319493-66-8 Structure
  • Basic information

    1. Product Name: 5-[2-(2-chloroethyl)phenyl]dihydrofuran-2-one
    2. Synonyms: 5-[2-(2-chloroethyl)phenyl]dihydrofuran-2-one
    3. CAS NO:319493-66-8
    4. Molecular Formula:
    5. Molecular Weight: 224.687
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 319493-66-8.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: 5-[2-(2-chloroethyl)phenyl]dihydrofuran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-[2-(2-chloroethyl)phenyl]dihydrofuran-2-one(319493-66-8)
    11. EPA Substance Registry System: 5-[2-(2-chloroethyl)phenyl]dihydrofuran-2-one(319493-66-8)
  • 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: 319493-66-8(Hazardous Substances Data)

319493-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 319493-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,9,4,9 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 319493-66:
(8*3)+(7*1)+(6*9)+(5*4)+(4*9)+(3*3)+(2*6)+(1*6)=168
168 % 10 = 8
So 319493-66-8 is a valid CAS Registry Number.

319493-66-8Downstream Products

319493-66-8Relevant articles and documents

Development of a protocol for eight- and nine-membered ring synthesis in the annulation of sp2,sp3-hybridized organic dihalides with keto esters

Molander,Kollner

, p. 8333 - 8339 (2000)

A protocol has been developed in which annulation reactions of various dihalides with keto esters can be carried out to provide entry to eight- and nine-membered carbocycles. In this process wherein one alkenyl- or aryl bromide and a tethered alkyl chloride comprise the organic dihalide, a selective metal - halogen exchange reaction between the sp2-hybridized bromide and an organolithium initiates the process. Transmetalation to an organoytterbium reagent generates a species that undergoes selective carbonyl addition to the ketone of the keto ester, creating a lactone intermediate. Subjection of the resulting chloroalkyl lactone to intramolecular reductive coupling with samarium(II) iodide completes the desired annulation.

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