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69769-79-5

1-(6-Methoxy-naphthalen-1-yl)-2-phenyl-ethane-1,2-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69769-79-5 Structure

  • Basic information

    1. Product Name: 1-(6-Methoxy-naphthalen-1-yl)-2-phenyl-ethane-1,2-dione
    2. Synonyms: 1-(6-Methoxy-naphthalen-1-yl)-2-phenyl-ethane-1,2-dione
    3. CAS NO:69769-79-5
    4. Molecular Formula:
    5. Molecular Weight: 290.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69769-79-5.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: 1-(6-Methoxy-naphthalen-1-yl)-2-phenyl-ethane-1,2-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(6-Methoxy-naphthalen-1-yl)-2-phenyl-ethane-1,2-dione(69769-79-5)
    11. EPA Substance Registry System: 1-(6-Methoxy-naphthalen-1-yl)-2-phenyl-ethane-1,2-dione(69769-79-5)

  • 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: 69769-79-5(Hazardous Substances Data)

69769-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69769-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,6 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69769-79:
(7*6)+(6*9)+(5*7)+(4*6)+(3*9)+(2*7)+(1*9)=205
205 % 10 = 5
So 69769-79-5 is a valid CAS Registry Number.

69769-79-5Downstream Products

69769-79-5Relevant articles and documents

Efficient syntheses of some 1-naphthylalkyl ketones and studies on their autooxidation in basic medium

Chatterjee,Raychaudhuri,Chatterjee

, p. 3653 - 3660 (1981)

Birch reductions of 4,6-dimethoxy-1-naphthylalkyl ketones 1 provided in fair to good yields the demethoxylated products, 6-methoxy-1-naphthylalkyl ketones 2(a-g), not easily accessible by other procedures. Autooxidation of these ketones in basic medium afforded the diketones 6(a-c), the acid 2h, and interestingly the phenol 5. Extension of this reduction to the related tricyclic ketone 8 afforded 9a, the phenolic ketone 9b; and significantly the dihydrocoumarin derivative 10 as a result of autooxidation of 9a. The mechanisms for demethoxylation and autooxidation have been discussed.

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