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CAS

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89937-61-1

N-(3'-hydroxybenzyl)hydroxylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89937-61-1 Structure

  • Basic information

    1. Product Name: N-(3'-hydroxybenzyl)hydroxylamine
    2. Synonyms:
    3. CAS NO:89937-61-1
    4. Molecular Formula:
    5. Molecular Weight: 139.154
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89937-61-1.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-(3'-hydroxybenzyl)hydroxylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3'-hydroxybenzyl)hydroxylamine(89937-61-1)
    11. EPA Substance Registry System: N-(3'-hydroxybenzyl)hydroxylamine(89937-61-1)

  • 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: 89937-61-1(Hazardous Substances Data)

89937-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89937-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,3 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89937-61:
(7*8)+(6*9)+(5*9)+(4*3)+(3*7)+(2*6)+(1*1)=201
201 % 10 = 1
So 89937-61-1 is a valid CAS Registry Number.

89937-61-1Downstream Products

89937-61-1Relevant articles and documents

Synthesis and tyrosinase inhibitory activity of novel N-hydroxybenzyl-N-nitrosohydroxylamines

Shiino, Mitsuhiro,Watanabe, Yumi,Umezawa, Kazuo

, p. 129 - 135 (2003)

Several novel N-substituted N-nitrosohydroxylamines were synthesized. They all inhibited mushroom tyrosinase, but the type of inhibition was different depending on the substituent. Some N-(mono- or dihydroxybenzyl)-N-nitrosohydroxylamines exhibited uncompetitive inhibition with respect to L-dopa. Among them, compound 6 was also a competitive inhibitor with respect to oxygen. This observation suggests that another interaction by the meta- or para-hydroxyl group might stabilize the binding of the inhibitor to the enzyme through the oxygen binding site.

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