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1332866-02-0

C21H18ClNO4S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1332866-02-0 Structure

  • Basic information

    1. Product Name: C21H18ClNO4S2
    2. Synonyms: C21H18ClNO4S2
    3. CAS NO:1332866-02-0
    4. Molecular Formula:
    5. Molecular Weight: 447.963
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1332866-02-0.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: C21H18ClNO4S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H18ClNO4S2(1332866-02-0)
    11. EPA Substance Registry System: C21H18ClNO4S2(1332866-02-0)

  • 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: 1332866-02-0(Hazardous Substances Data)

1332866-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332866-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,8,6 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1332866-02:
(9*1)+(8*3)+(7*3)+(6*2)+(5*8)+(4*6)+(3*6)+(2*0)+(1*2)=150
150 % 10 = 0
So 1332866-02-0 is a valid CAS Registry Number.

1332866-02-0Downstream Products

1332866-02-0Relevant articles and documents

Lewis base assisted Bronsted base catalysis: Direct regioselective asymmetric vinylogous alkylation of allylic sulfones

Jiang, Lin,Lei, Qian,Huang, Xin,Cui, Hai-Lei,Zhou, Xue,Chen, Ying-Chun

supporting information; experimental part, p. 9489 - 9493 (2011/09/16)

A Lewis base assisted Brnsted base catalysis (LBABB) strategy is applied for direct asymmetric vinylogous alkylation of allylic sulfones with Morita-Baylis-Hillman (MBH) carbonates, in which a strong Brnsted base, tert-butoxy anion, generated in situ from a tertiary amine catalyst and MBH carbonate, is crucial in activating unstabilized nucleophiles. The γ-regioselective alkylation products were obtained with good to excellent enantiomeric excess values when catalyzed by a modified cinchona alkaloid. Copyright

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