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156744-69-3

2-Allyl-3-methoxy-[1,4]benzoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156744-69-3 Structure

  • Basic information

    1. Product Name: 2-Allyl-3-methoxy-[1,4]benzoquinone
    2. Synonyms:
    3. CAS NO:156744-69-3
    4. Molecular Formula:
    5. Molecular Weight: 178.188
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156744-69-3.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: 2-Allyl-3-methoxy-[1,4]benzoquinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Allyl-3-methoxy-[1,4]benzoquinone(156744-69-3)
    11. EPA Substance Registry System: 2-Allyl-3-methoxy-[1,4]benzoquinone(156744-69-3)

  • 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: 156744-69-3(Hazardous Substances Data)

156744-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156744-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,4 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156744-69:
(8*1)+(7*5)+(6*6)+(5*7)+(4*4)+(3*4)+(2*6)+(1*9)=163
163 % 10 = 3
So 156744-69-3 is a valid CAS Registry Number.

156744-69-3Downstream Products

156744-69-3Relevant articles and documents

Ultrasound-promoted synthesis of substituted phenanthrene-1,4-quinones; the structure of plectranthon D

Zhang, Zhao-Rong,Flachsmann, Felix,Moghaddam, Firouz Matloubi,Rueedi, Peter

, p. 2153 - 2156 (1994)

A series of tanshinone-type diterpenoids was prepared by ultrasound-promoted and Lewis acid catalyzed, highly regioselective cycloadditions of styrenes with substituted 1,4-benzoquinones as the key step.

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