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CAS

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128766-70-1

Benzenesulfonyl-cyclopent-2-enyl-acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128766-70-1 Structure

  • Basic information

    1. Product Name: Benzenesulfonyl-cyclopent-2-enyl-acetonitrile
    2. Synonyms: Benzenesulfonyl-cyclopent-2-enyl-acetonitrile
    3. CAS NO:128766-70-1
    4. Molecular Formula:
    5. Molecular Weight: 247.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128766-70-1.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: Benzenesulfonyl-cyclopent-2-enyl-acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonyl-cyclopent-2-enyl-acetonitrile(128766-70-1)
    11. EPA Substance Registry System: Benzenesulfonyl-cyclopent-2-enyl-acetonitrile(128766-70-1)

  • 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: 128766-70-1(Hazardous Substances Data)

128766-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128766-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,7,6 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 128766-70:
(8*1)+(7*2)+(6*8)+(5*7)+(4*6)+(3*6)+(2*7)+(1*0)=161
161 % 10 = 1
So 128766-70-1 is a valid CAS Registry Number.

128766-70-1Relevant articles and documents

Palladium-catalyzed allylic alkylation of α-sulfinyl carbanions under biphasic conditions

Maitro, Guillaume,Prestat, Guillaume,Madec, David,Poli, Giovanni

, p. 1055 - 1058 (2006)

Palladium-catalyzed allylic alkylation of α-sulfinyl carbanions can take place under biphasic conditions. These new conditions provide a simple, mild and efficient route to allylated sulfoxides in good yields. The reaction tolerates a wide variety of EWG

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