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97783-05-6

4-Chloro-2-(hydroperoxy-phenylazo-methyl)-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97783-05-6 Structure

  • Basic information

    1. Product Name: 4-Chloro-2-(hydroperoxy-phenylazo-methyl)-phenol
    2. Synonyms: 4-Chloro-2-(hydroperoxy-phenylazo-methyl)-phenol
    3. CAS NO:97783-05-6
    4. Molecular Formula:
    5. Molecular Weight: 278.695
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97783-05-6.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: 4-Chloro-2-(hydroperoxy-phenylazo-methyl)-phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Chloro-2-(hydroperoxy-phenylazo-methyl)-phenol(97783-05-6)
    11. EPA Substance Registry System: 4-Chloro-2-(hydroperoxy-phenylazo-methyl)-phenol(97783-05-6)

  • 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: 97783-05-6(Hazardous Substances Data)

97783-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97783-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,8 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97783-05:
(7*9)+(6*7)+(5*7)+(4*8)+(3*3)+(2*0)+(1*5)=186
186 % 10 = 6
So 97783-05-6 is a valid CAS Registry Number.

97783-05-6Downstream Products

97783-05-6Relevant articles and documents

Intramolecular Catalysis of Oxygen Atom Transfer Reactions of α-Azo Hydroperoxides

Baumstark, Alfons L.,Vasquez, Pedro C.

, p. 3657 - 3659 (1985)

α-Azo hydroperoxides containing phenolic groups were 102 more reactive at epoxidetions and S-oxidation than electronically similar analugues due to intramolecular acid catalysis of the ionic oxidations.

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