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38105-20-3

Acetamide, N-hydroxy-N-1-naphthalenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38105-20-3 Structure

  • Basic information

    1. Product Name: Acetamide, N-hydroxy-N-1-naphthalenyl-
    2. Synonyms:
    3. CAS NO:38105-20-3
    4. Molecular Formula: C12H11NO2
    5. Molecular Weight: 201.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38105-20-3.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: Acetamide, N-hydroxy-N-1-naphthalenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-hydroxy-N-1-naphthalenyl-(38105-20-3)
    11. EPA Substance Registry System: Acetamide, N-hydroxy-N-1-naphthalenyl-(38105-20-3)

  • 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: 38105-20-3(Hazardous Substances Data)

38105-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38105-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,0 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38105-20:
(7*3)+(6*8)+(5*1)+(4*0)+(3*5)+(2*2)+(1*0)=93
93 % 10 = 3
So 38105-20-3 is a valid CAS Registry Number.

38105-20-3Relevant articles and documents

The Solvolysis of N-Acetoxy-1-N-acetylaminonaphtalene and N-Acetoxy-2-N-acetylaminonaphtalene: Divergent Chemistry and Mutagenic Activity

Underwood, Graham R.,Davidson, Catherine M.

, p. 555 - 556 (2007/10/02)

Upon solvolysis in neutral 40percent aqueous acetone, N-acetoxy-1-N- and N-acetoxy-2-N-acetylaminonaphtalene exibit completely different modes of reaction; the former reacts with nitrenium ion formation, while the latter undergoes acyl oxygen scission.

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