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CAS

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916085-15-9

Benzenesulfonamide, N-[1-(3-buten-1-yl)-2-butyl-2-cyclopenten-1-yl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 916085-15-9 Structure

  • Basic information

    1. Product Name: Benzenesulfonamide, N-[1-(3-buten-1-yl)-2-butyl-2-cyclopenten-1-yl]-4-methyl-
    2. Synonyms:
    3. CAS NO:916085-15-9
    4. Molecular Formula: C20H29NO2S
    5. Molecular Weight: 347.522
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 916085-15-9.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: Benzenesulfonamide, N-[1-(3-buten-1-yl)-2-butyl-2-cyclopenten-1-yl]-4-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonamide, N-[1-(3-buten-1-yl)-2-butyl-2-cyclopenten-1-yl]-4-methyl-(916085-15-9)
    11. EPA Substance Registry System: Benzenesulfonamide, N-[1-(3-buten-1-yl)-2-butyl-2-cyclopenten-1-yl]-4-methyl-(916085-15-9)

  • 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: 916085-15-9(Hazardous Substances Data)

916085-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 916085-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,0,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 916085-15:
(8*9)+(7*1)+(6*6)+(5*0)+(4*8)+(3*5)+(2*1)+(1*5)=169
169 % 10 = 9
So 916085-15-9 is a valid CAS Registry Number.

916085-15-9Relevant articles and documents

New route to azaspirocycles via the organolithium-mediated conversion of β-alkoxy aziridines into cyclopentenyl amines

Moore, Stephen P.,Coote, Susannah C.,O'Brien, Peter,Gilday, John

, p. 5145 - 5148 (2006)

(Chemical Equation Presented) A new three-step route to azaspirocycles involving the organolithium-mediated conversion of β-alkoxy aziridines into substituted cyclopentenyl amines, hydroboration, and cyclization has been developed. The methodology is util

Organolithium-mediated conversion of β-alkoxy aziridines into allylic sulfonamides: Effect of the N-sulfonyl group and a formal synthesis of (±)-perhydrohistrionicotoxin

Coote, Susannah C.,Moore, Stephen P.,O'Brien, Peter,Whitwood, Adrian C.,Gilday, John

, p. 7852 - 7855 (2008/12/22)

(Chemical Equation Presented) In 18 out of 20 examples of the organolithium-mediated conversion of β-alkoxy aziridines into substituted allylic sulfonamides, use of a Bus (Bus = t-BuSO2) substituent on the nitrogen gave higher yields compared t

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