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CAS

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72420-70-3

Cyclohexyldi-n-hexylmethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72420-70-3 Structure

  • Basic information

    1. Product Name: Cyclohexyldi-n-hexylmethanol
    2. Synonyms:
    3. CAS NO:72420-70-3
    4. Molecular Formula:
    5. Molecular Weight: 282.51
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72420-70-3.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: Cyclohexyldi-n-hexylmethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexyldi-n-hexylmethanol(72420-70-3)
    11. EPA Substance Registry System: Cyclohexyldi-n-hexylmethanol(72420-70-3)

  • 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: 72420-70-3(Hazardous Substances Data)

72420-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72420-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,2 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72420-70:
(7*7)+(6*2)+(5*4)+(4*2)+(3*0)+(2*7)+(1*0)=103
103 % 10 = 3
So 72420-70-3 is a valid CAS Registry Number.

72420-70-3Downstream Products

72420-70-3Relevant articles and documents

Improved synthesis of tertiary alcohols from reactions of organoboranes with 2-lithio-1,3-benzodithioles

Ncube, Smollie,Pelter, Andrew,Smith, Keith

, p. 1895 - 1896 (1979)

Treatment of trialkylboranes with 2-lithio-1,3-benzodithioles and then mercuric chloride (or methyl fluorosulhonate) followed by oxidation gives tertiary alcohols in high yields. The method is applicable to reactions of hindered organoboranes that fail using 1-lithio-1,1-bis(phenylthio)alkanes.

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