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536723-91-8

N-(5-tert-butyl-2-methoxy-phenyl)-hydroxylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 536723-91-8 Structure

  • Basic information

    1. Product Name: N-(5-tert-butyl-2-methoxy-phenyl)-hydroxylamine
    2. Synonyms: N-(5-tert-butyl-2-methoxy-phenyl)-hydroxylamine
    3. CAS NO:536723-91-8
    4. Molecular Formula:
    5. Molecular Weight: 195.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 536723-91-8.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: N-(5-tert-butyl-2-methoxy-phenyl)-hydroxylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(5-tert-butyl-2-methoxy-phenyl)-hydroxylamine(536723-91-8)
    11. EPA Substance Registry System: N-(5-tert-butyl-2-methoxy-phenyl)-hydroxylamine(536723-91-8)

  • 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: 536723-91-8(Hazardous Substances Data)

536723-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 536723-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,7,2 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 536723-91:
(8*5)+(7*3)+(6*6)+(5*7)+(4*2)+(3*3)+(2*9)+(1*1)=168
168 % 10 = 8
So 536723-91-8 is a valid CAS Registry Number.

536723-91-8Downstream Products

536723-91-8Relevant articles and documents

Condensations of N-arylhydroxylamines for the preparation of 5,5′-di-tert-butyl-2,2′-dihydroxydiphenylamine

Spence, John D.,Raymond, Ashley E.,Norton, Dianne E.

, p. 849 - 851 (2003)

Acid-promoted condensation of 4-tert-butyl-2-hydroxylaminoanisole with p-tert-butylphenol resulted in the formation of 5,5′-di-tert-butyl-2,2′-dihydroxydiphenylamine upon demethylation with BBr3. Protection of the acidic phenol unit was require

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