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1085390-04-0

(2R,3R)-1-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-aziridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1085390-04-0 Structure

  • Basic information

    1. Product Name: (2R,3R)-1-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-aziridine
    2. Synonyms: (2R,3R)-1-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-aziridine
    3. CAS NO:1085390-04-0
    4. Molecular Formula:
    5. Molecular Weight: 303.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1085390-04-0.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: (2R,3R)-1-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-aziridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-1-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-aziridine(1085390-04-0)
    11. EPA Substance Registry System: (2R,3R)-1-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-aziridine(1085390-04-0)

  • 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: 1085390-04-0(Hazardous Substances Data)

1085390-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1085390-04-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,5,3,9 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1085390-04:
(9*1)+(8*0)+(7*8)+(6*5)+(5*3)+(4*9)+(3*0)+(2*0)+(1*4)=150
150 % 10 = 0
So 1085390-04-0 is a valid CAS Registry Number.

1085390-04-0Relevant articles and documents

Readily available nitrene precursors increase the scope of Evans' asymmetric aziridination of olefins

Soedergren, Mikael J.,Alonso, Diego A.,Andersson, Pher G.

, p. 3563 - 3565 (1997)

The performance of the copper-catalyzed asymmetric aziridination of olefins is highly dependent on the properties of the nitrene precursor. Our preliminary results show significant improvements of both enantioselectivity and chemical yields when [N-(4-nitrobenzenesulfonyl)imino]phenyliodinane 1b (p-NO2C6H4SO2N=IPh) is employed instead of the commonly used p-tolyl analog 1a (PhI=NTs). This paper reports the comparison of some nitrene precursors for the copper-catalyzed asymmetric aziridination of olefins, utilizing the olefin as the limiting component and 1.5 equivalents of the nitrene precursor. The aziridine derivatives of several olefins were obtained in moderate to excellent yields and with enantioselectivity up to 95% ee.

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