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CAS

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162405-07-4

2-(4-Cyclohexylphenyl)-2-hydroxybutansaeure is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162405-07-4 Structure

  • Basic information

    1. Product Name: 2-(4-Cyclohexylphenyl)-2-hydroxybutansaeure
    2. Synonyms:
    3. CAS NO:162405-07-4
    4. Molecular Formula:
    5. Molecular Weight: 262.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 162405-07-4.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: 2-(4-Cyclohexylphenyl)-2-hydroxybutansaeure(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-Cyclohexylphenyl)-2-hydroxybutansaeure(162405-07-4)
    11. EPA Substance Registry System: 2-(4-Cyclohexylphenyl)-2-hydroxybutansaeure(162405-07-4)

  • 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: 162405-07-4(Hazardous Substances Data)

162405-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162405-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,4,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 162405-07:
(8*1)+(7*6)+(6*2)+(5*4)+(4*0)+(3*5)+(2*0)+(1*7)=104
104 % 10 = 4
So 162405-07-4 is a valid CAS Registry Number.

162405-07-4Relevant articles and documents

Synthesis and properties of 3-alkylsubstituted 1-alkoxy(hydroxy)indolin-2-ones

Geffken,Frobose

, p. 889 - 893 (2007/10/02)

N-alkoxy-2-aryl-2-hydroxycarboxamides 3 are smoothly converted into 3-alkylsubstituted 1-alkoxyindolin-2-ones (2A) by dicyclohexylcarbodiimide in boiling trichloroethene. The acidolysis of the 1-tert-butoxyindolin-2-ones 2Ab, g, i, k as well as the 1-alko

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