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858422-91-0

1-m-tolyl-cyclopent-3-enecarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 858422-91-0 Structure

  • Basic information

    1. Product Name: 1-m-tolyl-cyclopent-3-enecarbonitrile
    2. Synonyms: 1-m-tolyl-cyclopent-3-enecarbonitrile
    3. CAS NO:858422-91-0
    4. Molecular Formula:
    5. Molecular Weight: 183.253
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 858422-91-0.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: 1-m-tolyl-cyclopent-3-enecarbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-m-tolyl-cyclopent-3-enecarbonitrile(858422-91-0)
    11. EPA Substance Registry System: 1-m-tolyl-cyclopent-3-enecarbonitrile(858422-91-0)

  • 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: 858422-91-0(Hazardous Substances Data)

858422-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 858422-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,4,2 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 858422-91:
(8*8)+(7*5)+(6*8)+(5*4)+(4*2)+(3*2)+(2*9)+(1*1)=200
200 % 10 = 0
So 858422-91-0 is a valid CAS Registry Number.

858422-91-0Relevant articles and documents

Domino synthesis of fluorine-substituted polycyclic aromatic hydrocarbons: 1,1-difluoroallenes as synthetic platforms

Fuchibe, Kohei,Mayumi, Yuka,Zhao, Nan,Watanabe, Shumpei,Yokota, Misaki,Ichikawa, Junji

, p. 7825 - 7828 (2013)

Rather crafty: 1,1-Difluoroallenes bearing an aryl group and a cyclopentene moiety undergo indium(III)-catalyzed Friedel-Crafts-type cyclization with subsequent ring expansion and dehydrogenation to afford fluorinated polycyclic aromatic hydrocarbons in high yields. The introduction of an Ar group was effected by in situ halogenation of the intermediary indium species and a subsequent Suzuki-Miyaura reaction. Copyright

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