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898538-82-4

2-(3-hydroxy-propenyl)-4-methoxy-5-methyl-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 898538-82-4 Structure

  • Basic information

    1. Product Name: 2-(3-hydroxy-propenyl)-4-methoxy-5-methyl-phenol
    2. Synonyms: 2-(3-hydroxy-propenyl)-4-methoxy-5-methyl-phenol
    3. CAS NO:898538-82-4
    4. Molecular Formula:
    5. Molecular Weight: 194.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 898538-82-4.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-(3-hydroxy-propenyl)-4-methoxy-5-methyl-phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-hydroxy-propenyl)-4-methoxy-5-methyl-phenol(898538-82-4)
    11. EPA Substance Registry System: 2-(3-hydroxy-propenyl)-4-methoxy-5-methyl-phenol(898538-82-4)

  • 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: 898538-82-4(Hazardous Substances Data)

898538-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898538-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,5,3 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 898538-82:
(8*8)+(7*9)+(6*8)+(5*5)+(4*3)+(3*8)+(2*8)+(1*2)=254
254 % 10 = 4
So 898538-82-4 is a valid CAS Registry Number.

898538-82-4Relevant articles and documents

The synthesis of heliannuol C, an allelochemical from Helianthus annuus

Biswas, Bidyut,Sen, Prabir K.,Venkateswaran, Ramanathapuram V.

, p. 4019 - 4021 (2006)

The synthesis of the allelochemical heliannuol C 1 is described by employing a Bargellini condensation and a Claisen rearrangement to install the gem-dimethyl and vinyl functionalities, respectively. A Dieckmann cyclisation of diester 11 enabled the gener

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