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  • 56973-63-8 Structure
  • Basic information

    1. Product Name: C8H4O2
    2. Synonyms:
    3. CAS NO:56973-63-8
    4. Molecular Formula:
    5. Molecular Weight: 132.119
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56973-63-8.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: C8H4O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C8H4O2(56973-63-8)
    11. EPA Substance Registry System: C8H4O2(56973-63-8)
  • 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: 56973-63-8(Hazardous Substances Data)

56973-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56973-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,7 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56973-63:
(7*5)+(6*6)+(5*9)+(4*7)+(3*3)+(2*6)+(1*3)=168
168 % 10 = 8
So 56973-63-8 is a valid CAS Registry Number.

56973-63-8Upstream product

56973-63-8Relevant articles and documents

First measurements of absolute rate constants for oxacarbene intermediates produced in the photochemistry of benzocyclobutenedione

Boate,Johnston,Kwong,Lee-Ruff,Scaiano

, p. 8858 - 8863 (1990)

The photochemistry of benzocyclobutenedione in solution has been examined by use of laser flash photolysis techniques. Two rapid processes appear to compete. One leads to the formation of the long-lived bisketene IV, which can be readily observed (λmax 380 nm). The other process leads to oxacarbene III. This carbene could not be monitored directly, but probing techniques, with pyridine and adamantanethione as probes, lead to readily detectable ylides that can be employed to characterize the kinetic behavior of III. Thus, III lives about 20 μs in toluene and can be trapped by typical carbene scavengers such as alcohols. Carbene trapping by alcohols is in fact a complex reaction, since it also leads to equilibration with a short-lived intermediate (studied in detail in methanol/acetonitrile) that in turn can be trapped by alcohols, azides, and halides. This intermediate is tentatively assigned to carbocation VIII formed by solvent protonation of III.

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