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CAS

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79246-40-5

Pentanoic acid 2-cycloprop-2-enyl-2-oxo-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79246-40-5 Structure

  • Basic information

    1. Product Name: Pentanoic acid 2-cycloprop-2-enyl-2-oxo-ethyl ester
    2. Synonyms: Pentanoic acid 2-cycloprop-2-enyl-2-oxo-ethyl ester
    3. CAS NO:79246-40-5
    4. Molecular Formula:
    5. Molecular Weight: 182.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79246-40-5.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: Pentanoic acid 2-cycloprop-2-enyl-2-oxo-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pentanoic acid 2-cycloprop-2-enyl-2-oxo-ethyl ester(79246-40-5)
    11. EPA Substance Registry System: Pentanoic acid 2-cycloprop-2-enyl-2-oxo-ethyl ester(79246-40-5)

  • 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: 79246-40-5(Hazardous Substances Data)

79246-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79246-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,4 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79246-40:
(7*7)+(6*9)+(5*2)+(4*4)+(3*6)+(2*4)+(1*0)=155
155 % 10 = 5
So 79246-40-5 is a valid CAS Registry Number.

79246-40-5Downstream Products

79246-40-5Relevant articles and documents

A STUDY ON THE TRANSITION STATE IN THE PHOTOOXYGENATIONS BY AROMATIC AMINE N-OXIDES

Ogawa, Yuji,Iwasaki, Shigeo,Okuda, Shigenobu

, p. 2277 - 2280 (2007/10/02)

Oxygen-atom transfer process in the photolysis of aromatic amine N-oxides was suggested to involve the primary oxygen-atom elimination from N-oxides to give "oxene" followed by its reactions with the oxygen-acceptors.

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