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30839-37-3

3,8-Dimethoxy-1,2-naphthoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30839-37-3 Structure

  • Basic information

    1. Product Name: 3,8-Dimethoxy-1,2-naphthoquinone
    2. Synonyms: 3,8-Dimethoxy-1,2-naphthalenedione;3,8-Dimethoxy-1,2-naphthoquinone
    3. CAS NO:30839-37-3
    4. Molecular Formula: C12H10O4
    5. Molecular Weight: 218.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30839-37-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,8-Dimethoxy-1,2-naphthoquinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,8-Dimethoxy-1,2-naphthoquinone(30839-37-3)
    11. EPA Substance Registry System: 3,8-Dimethoxy-1,2-naphthoquinone(30839-37-3)

  • 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: 30839-37-3(Hazardous Substances Data)

30839-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30839-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,3 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30839-37:
(7*3)+(6*0)+(5*8)+(4*3)+(3*9)+(2*3)+(1*7)=113
113 % 10 = 3
So 30839-37-3 is a valid CAS Registry Number.

30839-37-3Relevant articles and documents

Laccase-generated quinones in naphthoquinone synthesis via Diels-Alder reaction

Witayakran, Suteera,Zettili, Abdullah,Ragauskas, Arthur J.

, p. 2983 - 2987 (2008/02/04)

The tandem synthesis of naphthoquinones was conducted from the reaction of laccase-generated quinones and acyclic dienes via Diels-Alder reaction. This reaction was carried out under mild condition in aqueous medium and yielded naphthoquinones up to 80%. In addition, the effect of solvent was also investigated and water was shown to be optimal for this reaction.

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