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30713-67-8

9,10-dihydro-9-methoxy-10-methylacridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30713-67-8 Structure

  • Basic information

    1. Product Name: 9,10-dihydro-9-methoxy-10-methylacridine
    2. Synonyms: 9,10-dihydro-9-methoxy-10-methylacridine
    3. CAS NO:30713-67-8
    4. Molecular Formula:
    5. Molecular Weight: 225.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30713-67-8.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: 9,10-dihydro-9-methoxy-10-methylacridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9,10-dihydro-9-methoxy-10-methylacridine(30713-67-8)
    11. EPA Substance Registry System: 9,10-dihydro-9-methoxy-10-methylacridine(30713-67-8)

  • 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: 30713-67-8(Hazardous Substances Data)

30713-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30713-67-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,1 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30713-67:
(7*3)+(6*0)+(5*7)+(4*1)+(3*3)+(2*6)+(1*7)=88
88 % 10 = 8
So 30713-67-8 is a valid CAS Registry Number.

30713-67-8Relevant articles and documents

Electrochemical Oxidative Aromatizationof 9-Substituted 9,10-Dihydroacridines: Cleavage of C–H vs C–X Bond

Chupakhin, Oleg N.,Shchepochkin, Alexander V.,Charushin, Valery N.,Maiorova, Anna V.,Kulikova, Tatyana V.,Shunyaev, Konstantin Yu.,Enyashin, Andrey N.,Slepukhin, Pavel A.,Suvorova, Anna I.

, p. 956 - 963 (2019)

[Figure not available: see fulltext.] Reactivity of dihydroacridines bearing a С–X fragment at the geminal C-9 atom (where X = C, N, O, P, S) on anode has been investigated by means of electrochemical oxidation and thermodynamic and quantum-chemical calculations. The electrochemical oxidation results either in the formation of the 9-substituted acridines or in the cleavage of the C–X bond. This dual behavior of dihydroazines is analogous to processes reported in literature that take place upon treatment with chemical oxidants.

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