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221123-48-4

3-(3-isopropyloxy-4-methoxyphenyl)propanol-1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 221123-48-4 Structure

  • Basic information

    1. Product Name: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1
    2. Synonyms: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1
    3. CAS NO:221123-48-4
    4. Molecular Formula:
    5. Molecular Weight: 224.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 221123-48-4.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: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1(221123-48-4)
    11. EPA Substance Registry System: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1(221123-48-4)

  • 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: 221123-48-4(Hazardous Substances Data)

221123-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221123-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,2 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 221123-48:
(8*2)+(7*2)+(6*1)+(5*1)+(4*2)+(3*3)+(2*4)+(1*8)=74
74 % 10 = 4
So 221123-48-4 is a valid CAS Registry Number.

221123-48-4Relevant articles and documents

A unified strategy toward the synthesis of acerogenin-type macrocycles: Total syntheses of acerogenins A, B, C, and L and aceroside IV

Islas Gonzalez, Gabriela,Zhu, Jieping

, p. 914 - 924 (2007/10/03)

A general strategy for the synthesis of acerogenin-type diarylheptanoids containing an endocyclic biaryl ether bond has been developed, and convergent total syntheses of acerogenin A, B, C, and L and aceroside IV have been accomplished. Cycloetherificatio

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