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Octanimidoyl chloride, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-N-(4-methoxyphenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 193477-02-0 Structure
  • Basic information

    1. Product Name: Octanimidoyl chloride, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-N-(4-methoxyphenyl)-, (Z)-
    2. Synonyms:
    3. CAS NO:193477-02-0
    4. Molecular Formula: C15H7ClF15NO
    5. Molecular Weight: 537.656
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 193477-02-0.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: Octanimidoyl chloride, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-N-(4-methoxyphenyl)-, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Octanimidoyl chloride, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-N-(4-methoxyphenyl)-, (Z)-(193477-02-0)
    11. EPA Substance Registry System: Octanimidoyl chloride, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluoro-N-(4-methoxyphenyl)-, (Z)-(193477-02-0)
  • 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: 193477-02-0(Hazardous Substances Data)

193477-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193477-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,7 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193477-02:
(8*1)+(7*9)+(6*3)+(5*4)+(4*7)+(3*7)+(2*0)+(1*2)=160
160 % 10 = 0
So 193477-02-0 is a valid CAS Registry Number.

193477-02-0Downstream Products

193477-02-0Relevant articles and documents

Facile preparation of polyfluoroalkylated aldimines from polyfluoroalkanoic acids

Takagi, Jun,Takihana, Ryozo,Kuwano, Akiko,Uneyama, Kenji

, p. 1624 - 1628 (2008/02/05)

Polyfluoroalkylated aldimines were prepared by reducing polyfluoroalkyl imidoyl chlorides, which are readily available from polyfluoroalkanoic acids, with LTBA (lithium tri-tert-butoxyaluminum hydride). Georg Thieme Verlag Stuttgart.

One-Pot Synthesis of Trifluoroacetimidoyl Halides

Tamura, Kenji,Mizukami, Hiromichi,Maeda, Kazuhiro,Watanabe, Hisayuki,Uneyama, Kenji

, p. 32 - 35 (2007/10/02)

Trifluoroacetimidoyl chlorides 1 were obtained in 80-90percent yields when a mixture of trifluoroacetic acid and a primary amine was heated in carbon tetrachloride in the presence of triphenylphosphine and triethylamine.The corresponding bromides 2 were o

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