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1322592-07-3

C24H20F2O6S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1322592-07-3 Structure

  • Basic information

    1. Product Name: C24H20F2O6S2
    2. Synonyms: C24H20F2O6S2
    3. CAS NO:1322592-07-3
    4. Molecular Formula:
    5. Molecular Weight: 506.548
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1322592-07-3.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: C24H20F2O6S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H20F2O6S2(1322592-07-3)
    11. EPA Substance Registry System: C24H20F2O6S2(1322592-07-3)

  • 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: 1322592-07-3(Hazardous Substances Data)

1322592-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1322592-07-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,2,5,9 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1322592-07:
(9*1)+(8*3)+(7*2)+(6*2)+(5*5)+(4*9)+(3*2)+(2*0)+(1*7)=133
133 % 10 = 3
So 1322592-07-3 is a valid CAS Registry Number.

1322592-07-3Downstream Products

1322592-07-3Relevant articles and documents

Highly enantio- and diastereoselective synthesis of β-methyl-γ- monofluoromethyl-substituted alcohols

Yang, Wenguo,Wei, Xinle,Pan, Yuanhang,Lee, Richmond,Zhu, Bo,Liu, Hongjun,Yan, Lin,Huang, Kuo-Wei,Jiang, Zhiyong,Tan, Choon-Hong

, p. 8066 - 8070 (2011)

Enanatiopure β-methyl-γ-monofluoromethyl alcohols were prepared from the allylic alkylation between fluorobis(phenylsulfonyl)methane with Morita-Baylis-Hillman carbonates. The reaction was catalyzed by using the Cinchona alkaloid derivative, (DHQD)2AQN. The origin of the stereoselectivity was verified by DFT methods. Calculated geometries and relative energies of various transition states strongly support the observed stereoselectivity.

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