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1028224-75-0

C22H34O5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1028224-75-0 Structure

  • Basic information

    1. Product Name: C22H34O5
    2. Synonyms: C22H34O5
    3. CAS NO:1028224-75-0
    4. Molecular Formula:
    5. Molecular Weight: 378.509
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1028224-75-0.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: C22H34O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H34O5(1028224-75-0)
    11. EPA Substance Registry System: C22H34O5(1028224-75-0)

  • 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: 1028224-75-0(Hazardous Substances Data)

1028224-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1028224-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,2,2 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1028224-75:
(9*1)+(8*0)+(7*2)+(6*8)+(5*2)+(4*2)+(3*4)+(2*7)+(1*5)=120
120 % 10 = 0
So 1028224-75-0 is a valid CAS Registry Number.

1028224-75-0Downstream Products

1028224-75-0Relevant articles and documents

An iodoetherification-dehydroiodination strategy for the synthesis of complex spiroketals from dihydroxyalkene precursors

Tony,Li, Xiaohua,Dabideen, Darrin,Li, Jialiang,Mootoo, David R.

supporting information; experimental part, p. 1165 - 1169 (2008/10/09)

Dihydroxyalkenes or their monoprotected alcohol derivatives are transformed to 5,5- and 5,6-spiroketals through a sequence involving an initial iodocyclization, followed by a silver triflate mediated spiroketalization step on the derived hydroxy-iodoether. This journal is The Royal Society of Chemistry.

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