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mesityl(2-methylprop-1-en-1-yl)iodonium trifluoromethanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1380240-10-7 Structure
  • Basic information

    1. Product Name: mesityl(2-methylprop-1-en-1-yl)iodonium trifluoromethanesulfonate
    2. Synonyms: mesityl(2-methylprop-1-en-1-yl)iodonium trifluoromethanesulfonate
    3. CAS NO:1380240-10-7
    4. Molecular Formula:
    5. Molecular Weight: 450.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380240-10-7.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: mesityl(2-methylprop-1-en-1-yl)iodonium trifluoromethanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: mesityl(2-methylprop-1-en-1-yl)iodonium trifluoromethanesulfonate(1380240-10-7)
    11. EPA Substance Registry System: mesityl(2-methylprop-1-en-1-yl)iodonium trifluoromethanesulfonate(1380240-10-7)
  • 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: 1380240-10-7(Hazardous Substances Data)

1380240-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380240-10-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,2,4 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1380240-10:
(9*1)+(8*3)+(7*8)+(6*0)+(5*2)+(4*4)+(3*0)+(2*1)+(1*0)=117
117 % 10 = 7
So 1380240-10-7 is a valid CAS Registry Number.

1380240-10-7Relevant articles and documents

Copper-Catalyzed Cross-Coupling of Vinyliodonium Salts and Zinc-Based Silicon Nucleophiles

Zhang, Liangliang,Oestreich, Martin

, p. 8061 - 8063 (2018)

A silylation of vinyliodonium salts using zinc-based silicon reagents as nucleophiles is reported. This cross-coupling is catalyzed by copper, and vinylsilanes are obtained in high yield likely following a Cu(I)/Cu(III) reaction mechanism. The procedure i

Enantioselective α-vinylation of aldehydes via the synergistic combination of copper and amine catalysis

Skucas, Eduardas,MacMillan, David W. C.

supporting information; experimental part, p. 9090 - 9093 (2012/07/14)

The enantioselective α-vinylation of aldehydes using vinyl iodonium triflate salts has been accomplished via the synergistic combination of copper and chiral amine catalysis. These mild catalytic conditions provide a direct route for the enantioselective construction of enolizable α-formyl vinylic stereocenters without racemization or olefin transposition. These high-value coupling adducts are readily converted into a variety of useful olefin synthons.

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