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1146906-80-0

(S)-1-[1-(tert-butylperoxy)-2-nitroethyl]-2-methylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1146906-80-0 Structure

  • Basic information

    1. Product Name: (S)-1-[1-(tert-butylperoxy)-2-nitroethyl]-2-methylbenzene
    2. Synonyms:
    3. CAS NO:1146906-80-0
    4. Molecular Formula:
    5. Molecular Weight: 253.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1146906-80-0.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: (S)-1-[1-(tert-butylperoxy)-2-nitroethyl]-2-methylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-[1-(tert-butylperoxy)-2-nitroethyl]-2-methylbenzene(1146906-80-0)
    11. EPA Substance Registry System: (S)-1-[1-(tert-butylperoxy)-2-nitroethyl]-2-methylbenzene(1146906-80-0)

  • 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: 1146906-80-0(Hazardous Substances Data)

1146906-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146906-80-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,9,0 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1146906-80:
(9*1)+(8*1)+(7*4)+(6*6)+(5*9)+(4*0)+(3*6)+(2*8)+(1*0)=160
160 % 10 = 0
So 1146906-80-0 is a valid CAS Registry Number.

1146906-80-0Downstream Products

1146906-80-0Relevant articles and documents

Catalytic asymmetric β-peroxidation of nitroalkenes

Russo, Alessio,Lattanzi, Alessandra

, p. 1991 - 1995 (2008)

The first example of an asymmetric β-peroxidation of nitroalkenes is disclosed. The reaction is promoted by catalytic loadings of a commercially available diaryl-2-pyrrolidinemethanol derivative and tert-butyl hydroperoxide as the oxidant. A synthetically useful class of peroxides is obtained in good yield and enantioselectivity (up to 84% ee).

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