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1072824-01-1

(4-hydroxy-6-methoxy-2-methylnaphthalen-1-yl) phenyl ketone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1072824-01-1 Structure

  • Basic information

    1. Product Name: (4-hydroxy-6-methoxy-2-methylnaphthalen-1-yl) phenyl ketone
    2. Synonyms: (4-hydroxy-6-methoxy-2-methylnaphthalen-1-yl) phenyl ketone
    3. CAS NO:1072824-01-1
    4. Molecular Formula:
    5. Molecular Weight: 292.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1072824-01-1.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: (4-hydroxy-6-methoxy-2-methylnaphthalen-1-yl) phenyl ketone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-hydroxy-6-methoxy-2-methylnaphthalen-1-yl) phenyl ketone(1072824-01-1)
    11. EPA Substance Registry System: (4-hydroxy-6-methoxy-2-methylnaphthalen-1-yl) phenyl ketone(1072824-01-1)

  • 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: 1072824-01-1(Hazardous Substances Data)

1072824-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1072824-01-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,8,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1072824-01:
(9*1)+(8*0)+(7*7)+(6*2)+(5*8)+(4*2)+(3*4)+(2*0)+(1*1)=131
131 % 10 = 1
So 1072824-01-1 is a valid CAS Registry Number.

1072824-01-1Downstream Products

1072824-01-1Relevant articles and documents

Gold-catalyzed hydrative carbocyclization of 1,5- and 1,6-diyn-3-ones via an oxygen transfer process

Tang, Jhih-Meng,Liu, Ting-An,Liu, Rai-Shung

, p. 8479 - 8483 (2008)

(Chemical Equation Presented) This study reports new hydrative carbocyclizations of 1,5- and 1,6-diyn-3-ones catalyzed by PPh3AuOTf, involving a π-alkyne-assisted oxygen transfer in the reaction mechanisms. Treatment of 2-(alk-2-yn-1-onyl)-1-alkynylbenzenes with PPh3AuOTf (5 mol %) in wet 1,4-dioxane (23°C, 10 min) led to hydrative aromatization to give 4-hydroxyl-1-naphthyl ketones efficiently. This approach is also extendible to the hydrative cyclization of acyclic 1,5-diyn-3-ones, which afforded 4-cyclopentenonyl ketones in reasonable yields. On the basis of this oxygen-labeling study, we propose a plausible mechanism involving an alkyne-assisted oxygen transfer to generate key oxonium and gold-enolate intermediates.

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