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906739-82-0

Benzeneacetic acid, 2-[[(trifluoromethyl)sulfonyl]oxy]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Benzeneacetic acid, 2-[[(trifluoromethyl)sulfonyl]oxy]-, methyl ester

    Cas No: 906739-82-0

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  • 906739-82-0 Structure

  • Basic information

    1. Product Name: Benzeneacetic acid, 2-[[(trifluoromethyl)sulfonyl]oxy]-, methyl ester
    2. Synonyms:
    3. CAS NO:906739-82-0
    4. Molecular Formula: C10H9F3O5S
    5. Molecular Weight: 298.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 906739-82-0.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: Benzeneacetic acid, 2-[[(trifluoromethyl)sulfonyl]oxy]-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetic acid, 2-[[(trifluoromethyl)sulfonyl]oxy]-, methyl ester(906739-82-0)
    11. EPA Substance Registry System: Benzeneacetic acid, 2-[[(trifluoromethyl)sulfonyl]oxy]-, methyl ester(906739-82-0)

  • 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: 906739-82-0(Hazardous Substances Data)

906739-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 906739-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,7,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 906739-82:
(8*9)+(7*0)+(6*6)+(5*7)+(4*3)+(3*9)+(2*8)+(1*2)=200
200 % 10 = 0
So 906739-82-0 is a valid CAS Registry Number.

906739-82-0Relevant articles and documents

Diversity synthesis using the complimentary reactivity of rhodium(II)- and palladium(II)-catalyzed reactions

Ni, Aiwu,France, Jessica E.,Davies, Huw M. L.

, p. 5594 - 5598 (2007/10/03)

Rhodium(II)-catalyzed reactions of aryldiazoacetates can be conducted in the presence of iodide, triflate, organoboron, and organostannane functionality, resulting in the formation of a variety of cyclopropanes or C-H insertion products with high stereoselectivity. The combination of the rhodium(II)-catalyzed reaction with a subsequent palladium(II)-catalyzed Suzuki coupling offers a novel strategy for diversity synthesis.

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