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790693-18-4

trans-5-cyclohexyl-4-iodopent-4-en-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 790693-18-4 Structure

  • Basic information

    1. Product Name: trans-5-cyclohexyl-4-iodopent-4-en-2-ol
    2. Synonyms:
    3. CAS NO:790693-18-4
    4. Molecular Formula:
    5. Molecular Weight: 294.176
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 790693-18-4.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: trans-5-cyclohexyl-4-iodopent-4-en-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-5-cyclohexyl-4-iodopent-4-en-2-ol(790693-18-4)
    11. EPA Substance Registry System: trans-5-cyclohexyl-4-iodopent-4-en-2-ol(790693-18-4)

  • 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: 790693-18-4(Hazardous Substances Data)

790693-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 790693-18-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,6,9 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 790693-18:
(8*7)+(7*9)+(6*0)+(5*6)+(4*9)+(3*3)+(2*1)+(1*8)=204
204 % 10 = 4
So 790693-18-4 is a valid CAS Registry Number.

790693-18-4Downstream Products

790693-18-4Relevant articles and documents

Stereocontrolled formation of vinylsilanes via homolytic substitution at silicon

Blum, Andreas,Hess, Wilfried,Studer, Armido

, p. 2226 - 2235 (2007/10/03)

Intramolecular homolytic substitution reactions at silicon by vinyl radicals are described. The reaction can be used for the formation of 5- and 6-membered cyclic alkoxysilanes bearing a vinyl silane functionality. These processes provide a new entry into highly substituted vinyl silanes. The reactions occur with moderate to excellent selectivities.

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