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Benzofuran, 2-(4-methoxyphenyl)-3-methyl-5-(1-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 568593-04-4 Structure
  • Basic information

    1. Product Name: Benzofuran, 2-(4-methoxyphenyl)-3-methyl-5-(1-propenyl)-
    2. Synonyms:
    3. CAS NO:568593-04-4
    4. Molecular Formula: C19H18O2
    5. Molecular Weight: 278.351
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 568593-04-4.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: Benzofuran, 2-(4-methoxyphenyl)-3-methyl-5-(1-propenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzofuran, 2-(4-methoxyphenyl)-3-methyl-5-(1-propenyl)-(568593-04-4)
    11. EPA Substance Registry System: Benzofuran, 2-(4-methoxyphenyl)-3-methyl-5-(1-propenyl)-(568593-04-4)
  • 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: 568593-04-4(Hazardous Substances Data)

568593-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 568593-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,8,5,9 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 568593-04:
(8*5)+(7*6)+(6*8)+(5*5)+(4*9)+(3*3)+(2*0)+(1*4)=204
204 % 10 = 4
So 568593-04-4 is a valid CAS Registry Number.

568593-04-4Relevant articles and documents

2,3-Disubstituted 2,3,5-trisubstituted benzofurans by regioselective Pd-catalyzed cross-coupling reactions; a short synthesis of eupomatenoid-15

Bach,Bartels

, p. 1284 - 1286 (2007/10/03)

2,3-Dibromobenzofuran (1) 2,3,5-tribromobenzofuran (2) undergo regioselective Sonogashira- Negishi-type cross-coupling reactions at the 2-position. Subsequent substitution reactions at C-3 are possible for the cross-coupling products obtained from compoun

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