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132279-99-3

dihydro-3-phenyl-5-acetoxymethyl-2(3H)-furanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132279-99-3 Structure

  • Basic information

    1. Product Name: dihydro-3-phenyl-5-acetoxymethyl-2(3H)-furanone
    2. Synonyms:
    3. CAS NO:132279-99-3
    4. Molecular Formula:
    5. Molecular Weight: 234.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132279-99-3.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: dihydro-3-phenyl-5-acetoxymethyl-2(3H)-furanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: dihydro-3-phenyl-5-acetoxymethyl-2(3H)-furanone(132279-99-3)
    11. EPA Substance Registry System: dihydro-3-phenyl-5-acetoxymethyl-2(3H)-furanone(132279-99-3)

  • 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: 132279-99-3(Hazardous Substances Data)

132279-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132279-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,7 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132279-99:
(8*1)+(7*3)+(6*2)+(5*2)+(4*7)+(3*9)+(2*9)+(1*9)=133
133 % 10 = 3
So 132279-99-3 is a valid CAS Registry Number.

132279-99-3Downstream Products

132279-99-3Relevant articles and documents

IODINE (III) MEDIATED ACETOXY-LACTONIZATION OF UNSATURATED NITRILES

Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco,Bartoli, Donatella

, p. 7139 - 7150 (1990)

4-Pentenenitriles reacted with PhI(OAc)2 in acetic acid, in the presence of 48percent HBF4, at 70 deg C, to afford the dihydro-5-acetoxymethyl-2(3H)-furanones in good yields.Similarly, 3-butenenitriles gave the dihydro-4-acetoxy-2(3H)-furanones, although in lower yields.Parallel experiments showed that, under the same conditions, 4-pentenoic and 3-pentenoic acids reacted much more easily and gave the same acetoxy-lactonization process at room temperature.

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