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1133467-72-7

[N-(trifluoromethanesulfonyl)imino](2-methylphenyl)-λ3-iodane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1133467-72-7 Structure

  • Basic information

    1. Product Name: [N-(trifluoromethanesulfonyl)imino](2-methylphenyl)-λ3-iodane
    2. Synonyms: [N-(trifluoromethanesulfonyl)imino](2-methylphenyl)-λ3-iodane
    3. CAS NO:1133467-72-7
    4. Molecular Formula:
    5. Molecular Weight: 365.115
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1133467-72-7.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: [N-(trifluoromethanesulfonyl)imino](2-methylphenyl)-λ3-iodane(CAS DataBase Reference)
    10. NIST Chemistry Reference: [N-(trifluoromethanesulfonyl)imino](2-methylphenyl)-λ3-iodane(1133467-72-7)
    11. EPA Substance Registry System: [N-(trifluoromethanesulfonyl)imino](2-methylphenyl)-λ3-iodane(1133467-72-7)

  • 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: 1133467-72-7(Hazardous Substances Data)

1133467-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1133467-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,4,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1133467-72:
(9*1)+(8*1)+(7*3)+(6*3)+(5*4)+(4*6)+(3*7)+(2*7)+(1*2)=137
137 % 10 = 7
So 1133467-72-7 is a valid CAS Registry Number.

1133467-72-7Downstream Products

1133467-72-7Relevant articles and documents

Imido transfer of sulfonylimino-λ3-bromane makes possible the synthesis of sulfonylimino-λ3-iodanes

Ochiai, Masahito,Nakano, Aiko,Yoshimura, Akira,Miyamoto, Kazunori,Hayashi, Satoko,Nakanishi, Waro

supporting information; experimental part, p. 959 - 961 (2009/07/10)

Sulfonylimino-λ3-bromane functions as a reactive nitrenoid, because of the hyperleaving group ability of aryl- λ3-bromanyl groups, and undergoes transimidations to iodobenzenes at room temperature under metal-free conditions probably

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