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Benzenemethanesulfenamide, a-(chlorophenylmethylene)-N,N-bis(trimethylsilyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Benzenemethanesulfenamide, a-(chlorophenylmethylene)-N,N-bis(trimethylsilyl)-, (E)-

    Cas No: 144216-66-0

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  • 144216-66-0 Structure
  • Basic information

    1. Product Name: Benzenemethanesulfenamide, a-(chlorophenylmethylene)-N,N-bis(trimethylsilyl)-, (E)-
    2. Synonyms:
    3. CAS NO:144216-66-0
    4. Molecular Formula: C20H28ClNSSi2
    5. Molecular Weight: 406.139
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144216-66-0.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: Benzenemethanesulfenamide, a-(chlorophenylmethylene)-N,N-bis(trimethylsilyl)-, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanesulfenamide, a-(chlorophenylmethylene)-N,N-bis(trimethylsilyl)-, (E)-(144216-66-0)
    11. EPA Substance Registry System: Benzenemethanesulfenamide, a-(chlorophenylmethylene)-N,N-bis(trimethylsilyl)-, (E)-(144216-66-0)
  • 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: 144216-66-0(Hazardous Substances Data)

144216-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144216-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,1 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 144216-66:
(8*1)+(7*4)+(6*4)+(5*2)+(4*1)+(3*6)+(2*6)+(1*6)=110
110 % 10 = 0
So 144216-66-0 is a valid CAS Registry Number.

144216-66-0Downstream Products

144216-66-0Relevant articles and documents

Phthalimidesulfenyl Chloride. Part 4. Addition to Acetylenes and Synthetic Utilization of their Adducts

Capozzi, Giuseppe,Gori, Luciano,Menichetti, Stefano,Nativi, Cristina

, p. 1923 - 1928 (2007/10/02)

Both the stereo- and regio-chemical reactivity of the phthalimidesulfenyl chloride 1 towards symmetrical and terminal acetylenes and the reactivity of the adducts 3 and 5 with various nucleophiles has been investigated.Nucleophilic substitution of the phthalimide residue was achieved with MeLi, PhLi, ButLi, (Me3Si)2NNa and Me3SiSMe.The synthesis of β-chlorovinyl tributylstannyl sulfides 14 is also described.The synthetic potential of the new sulfur compounds is discussed.

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