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70165-53-6

2,2-dimethoxy-3-chloro-5-tert-butylcyclohexanone oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 70165-53-6 Structure

  • Basic information

    1. Product Name: 2,2-dimethoxy-3-chloro-5-tert-butylcyclohexanone oxime
    2. Synonyms: 2,2-dimethoxy-3-chloro-5-tert-butylcyclohexanone oxime
    3. CAS NO:70165-53-6
    4. Molecular Formula:
    5. Molecular Weight: 263.765
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 70165-53-6.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: 2,2-dimethoxy-3-chloro-5-tert-butylcyclohexanone oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dimethoxy-3-chloro-5-tert-butylcyclohexanone oxime(70165-53-6)
    11. EPA Substance Registry System: 2,2-dimethoxy-3-chloro-5-tert-butylcyclohexanone oxime(70165-53-6)

  • 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: 70165-53-6(Hazardous Substances Data)

70165-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70165-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70165-53:
(7*7)+(6*0)+(5*1)+(4*6)+(3*5)+(2*5)+(1*3)=106
106 % 10 = 6
So 70165-53-6 is a valid CAS Registry Number.

70165-53-6Downstream Products

70165-53-6Relevant articles and documents

Reactions of 2,2-Dialkoxy Ketone Oximes with Chlorine and Bromine. Halogenation vs. Beckmann Fragmentation

Oxenrider, Bryce C.,Rogic, Milorad M.

, p. 2629 - 2633 (1982)

Reactions of 2,2-dialkoxycycloalkanone oximes with chlorine or bromine can be direct either to give 3-chloro- or 3-bromo-2,2-dialkoxycycloalkanone oximes or to undergo Beckmann fragmentation to give ω-(alkoxycarbonyl)alkanehydroximoyl halides.The resultin

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