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(2S,4aR)-2,4a-Dimethoxy-2,4a-dihydro-naphtho[2,1-c][1,2]dioxine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80405-33-0 Structure
  • Basic information

    1. Product Name: (2S,4aR)-2,4a-Dimethoxy-2,4a-dihydro-naphtho[2,1-c][1,2]dioxine
    2. Synonyms:
    3. CAS NO:80405-33-0
    4. Molecular Formula:
    5. Molecular Weight: 246.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80405-33-0.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: (2S,4aR)-2,4a-Dimethoxy-2,4a-dihydro-naphtho[2,1-c][1,2]dioxine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,4aR)-2,4a-Dimethoxy-2,4a-dihydro-naphtho[2,1-c][1,2]dioxine(80405-33-0)
    11. EPA Substance Registry System: (2S,4aR)-2,4a-Dimethoxy-2,4a-dihydro-naphtho[2,1-c][1,2]dioxine(80405-33-0)
  • 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: 80405-33-0(Hazardous Substances Data)

80405-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80405-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,0 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80405-33:
(7*8)+(6*0)+(5*4)+(4*0)+(3*5)+(2*3)+(1*3)=100
100 % 10 = 0
So 80405-33-0 is a valid CAS Registry Number.

80405-33-0Relevant articles and documents

THE 1,4-ADDITION OF SINGLET OXYGEN TO 2,6-DIMETHOXY-1-(2-METHOXYETHENYL)-BENZENE AND 2-METHOXY-1-(2-METHOXYETHENYL)NAPHTHALENE. THE 1,4-ENDO-PEROXIDES AS EQUIVALENTS OF 6-OXO-2,4-CYCLOHEXADIENYLIDENACETATES.

Matsumoto, Masakatsu,Kuroda, Keiko,Suzuki, Yoshito

, p. 3253 - 3256 (1981)

The sensitized photooxygenation of vinylarenes 1 and 2 gave the corresponding 1,4-endoperoxides which were decomposed under mild conditions into quinone methides bearing ester function at the exocyclic carbon.

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