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CAS

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486413-05-2

Aziridine, 1-[(4-methylphenyl)sulfonyl]-2-[4-[(trimethylsilyl)methyl]-4-pentenyl]-, (2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 486413-05-2 Structure

  • Basic information

    1. Product Name: Aziridine, 1-[(4-methylphenyl)sulfonyl]-2-[4-[(trimethylsilyl)methyl]-4-pentenyl]-, (2R)-
    2. Synonyms:
    3. CAS NO:486413-05-2
    4. Molecular Formula: C18H29NO2SSi
    5. Molecular Weight: 351.585
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 486413-05-2.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: Aziridine, 1-[(4-methylphenyl)sulfonyl]-2-[4-[(trimethylsilyl)methyl]-4-pentenyl]-, (2R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Aziridine, 1-[(4-methylphenyl)sulfonyl]-2-[4-[(trimethylsilyl)methyl]-4-pentenyl]-, (2R)-(486413-05-2)
    11. EPA Substance Registry System: Aziridine, 1-[(4-methylphenyl)sulfonyl]-2-[4-[(trimethylsilyl)methyl]-4-pentenyl]-, (2R)-(486413-05-2)

  • 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: 486413-05-2(Hazardous Substances Data)

486413-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 486413-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,4,1 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 486413-05:
(8*4)+(7*8)+(6*6)+(5*4)+(4*1)+(3*3)+(2*0)+(1*5)=162
162 % 10 = 2
So 486413-05-2 is a valid CAS Registry Number.

486413-05-2Relevant articles and documents

Aziridine-allylsilane-mediated synthesis of exocyclic γ-amino olefins and azabicyclo[x.y.1]-systems

Lapinsky, David J,Bergmeier, Stephen C

, p. 7109 - 7117 (2007/10/03)

We have shown that connection of C-2 of an allylsilane to a tethered aziridine ring yields exocyclic γ-amino olefins and desilylated azabicyclo[x.2.1]-systems upon cyclization with BF3·OEt2. Furthermore, manipulation of a specific exocyclic γ-amino olefin provided access to an azabicyclo[3.3.1]nonane. This methodology should be useful for the preparation of natural products and pharmacologically active agents containing these bicyclic heterocyclic systems.

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