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Diazene, cyclohexylphenyl-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52123-66-7 Structure
  • Basic information

    1. Product Name: Diazene, cyclohexylphenyl-, 2-oxide
    2. Synonyms:
    3. CAS NO:52123-66-7
    4. Molecular Formula: C12H16N2O
    5. Molecular Weight: 204.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52123-66-7.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: Diazene, cyclohexylphenyl-, 2-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Diazene, cyclohexylphenyl-, 2-oxide(52123-66-7)
    11. EPA Substance Registry System: Diazene, cyclohexylphenyl-, 2-oxide(52123-66-7)
  • 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: 52123-66-7(Hazardous Substances Data)

52123-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52123-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,2 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52123-66:
(7*5)+(6*2)+(5*1)+(4*2)+(3*3)+(2*6)+(1*6)=87
87 % 10 = 7
So 52123-66-7 is a valid CAS Registry Number.

52123-66-7Downstream Products

52123-66-7Relevant articles and documents

Oxidation of Aromatic Amines with Hydrogen Peroxide Catalyzed by Cetylpyridinium Heteropolyoxometalates

Sakaue, Sigeki,Tsubakino, Takashi,Nishiyama, Yutaka,Ishii, Yasutaka

, p. 3633 - 3638 (1993)

Various substituted anilines 1 were selectively converted into the corresponsing nitrosobenzenes 2 or nitrobenzenes 3 by oxidation with aqueous hydrogen peroxide catalyzed by heteropolyoxometalates.The oxidation of anilines 1 with 35percent H2O2 catalyzed by peroxotungstophosphate (PCWP) at room temperature in chloroform under two-phase conditions afforded nitrosobenzene 2 with high selectivity.When the same reactions were carried out at higher temperature (e.g., refluxing chloroform), nitrobenzenes 3 were obtained in good yields.The oxidation of aniline (1a) with dilute H2O2 catalyzed by PCWP (2 wtpercent) in an aqueous medium produced azoxybenzene (4a) with high selectivity.Phenylazoxyalkanes 7 were prepared by the first direct cooxidation of 1a in the presence of primary aliphatic amines 6.For example, the oxidation of a 1:2 mixture of 1a and hexylamine (6b) with 35percent H2O2 (6 equiv) in the presence of PCWP produced phenylazoxyhexane (7b) along with a small amount of 4a (8percent).The reaction path for the conversion of anilines to azoxy-, nitroso-, and nitrobenzenes is described.

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