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CAS

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13194-02-0

Cyclohexanone, O-(2,4,6-trinitrophenyl)oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13194-02-0 Structure

  • Basic information

    1. Product Name: Cyclohexanone, O-(2,4,6-trinitrophenyl)oxime
    2. Synonyms:
    3. CAS NO:13194-02-0
    4. Molecular Formula: C12H12N4O7
    5. Molecular Weight: 324.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13194-02-0.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: Cyclohexanone, O-(2,4,6-trinitrophenyl)oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanone, O-(2,4,6-trinitrophenyl)oxime(13194-02-0)
    11. EPA Substance Registry System: Cyclohexanone, O-(2,4,6-trinitrophenyl)oxime(13194-02-0)

  • 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: 13194-02-0(Hazardous Substances Data)

13194-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13194-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,9 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13194-02:
(7*1)+(6*3)+(5*1)+(4*9)+(3*4)+(2*0)+(1*2)=80
80 % 10 = 0
So 13194-02-0 is a valid CAS Registry Number.

13194-02-0Relevant articles and documents

Structure correlation study of the beckmann rearrangement: X-ray structural analysis and 13C-13C 1-bond coupling constant study of a range of cyclohexanone oxime derivatives

Yeoh, Shin Dee,Harris, Benjamin L.,Simons, Tristan J.,White, Jonathan M.

experimental part, p. 905 - 917 (2012/09/22)

The X-ray structures of a range of oxime derivatives (1 and 4), of cyclohexanone and 4-tert-butylcyclohexanone, where the electron demand of the oxygenated substituent on the oxime nitrogen (OR) is systematically varied were determined. It was established

Oxime ethers and pesticidal preparations containing them

-

, (2008/06/13)

New oxime ethers and pesticidal and herbicidal preparations containing them are disclosed. The oxime ethers correspond to the formula SPC1 Wherein R1 is a hydrogen atom or a lower alkyl radical; R2 is an aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic radical; or wherein R1 and R2 form part of a saturated or unsaturated carbocycle or a 5-, 6- or 7-membered heterocycle; R3 is nitro, trifluoromethyl, formyl, lower carbalkoxy, sulfamyl or mono- or di-lower alkyl fulfamyl radical; R4- and R5 each is a hydrogen or halogen atom, an amino, mono- or di-lower alkyl amino, lower alkoxy, cycloalkoxy, lower alkylthio, nitro, lower carbalkoxy, arylthio, lower aralkylthio or lower alkyl group, or 5-, 6- or 7-membered heterocycle.

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