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1345024-11-4

1,3-dimethoxy-2-methyl-5-[(Z)-prop-1-enyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1345024-11-4 Structure

  • Basic information

    1. Product Name: 1,3-dimethoxy-2-methyl-5-[(Z)-prop-1-enyl]benzene
    2. Synonyms: 1,3-dimethoxy-2-methyl-5-[(Z)-prop-1-enyl]benzene
    3. CAS NO:1345024-11-4
    4. Molecular Formula:
    5. Molecular Weight: 192.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1345024-11-4.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: 1,3-dimethoxy-2-methyl-5-[(Z)-prop-1-enyl]benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-dimethoxy-2-methyl-5-[(Z)-prop-1-enyl]benzene(1345024-11-4)
    11. EPA Substance Registry System: 1,3-dimethoxy-2-methyl-5-[(Z)-prop-1-enyl]benzene(1345024-11-4)

  • 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: 1345024-11-4(Hazardous Substances Data)

1345024-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1345024-11-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,0,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1345024-11:
(9*1)+(8*3)+(7*4)+(6*5)+(5*0)+(4*2)+(3*4)+(2*1)+(1*1)=114
114 % 10 = 4
So 1345024-11-4 is a valid CAS Registry Number.

1345024-11-4Relevant articles and documents

Total syntheses of (+)-pestaphthalide A and (-)-pestaphthalide B

Schwaben, Jonas,Cordes, Jens,Harms, Klaus,Koert, Ulrich

, p. 2929 - 2934 (2011/10/30)

Total syntheses of (+)-pestaphthalide A and (-)-pestaphthalide B were achieved. Key steps are an iridium-mediated meta-selective arylborylation, a Suzuki-coupling/Jacobsen-epoxidation sequence, a stereodivergent epoxide opening and an anionic cyclic carbonate/-lactone rearrangement. Georg Thieme Verlag Stuttgart - New York.

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