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1091629-60-5

(S)-3-(fluorobis(phenylsulfonyl)methyl)-1-phenylpentan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1091629-60-5 Structure

  • Basic information

    1. Product Name: (S)-3-(fluorobis(phenylsulfonyl)methyl)-1-phenylpentan-1-one
    2. Synonyms: (S)-3-(fluorobis(phenylsulfonyl)methyl)-1-phenylpentan-1-one
    3. CAS NO:1091629-60-5
    4. Molecular Formula:
    5. Molecular Weight: 474.574
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1091629-60-5.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: (S)-3-(fluorobis(phenylsulfonyl)methyl)-1-phenylpentan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-(fluorobis(phenylsulfonyl)methyl)-1-phenylpentan-1-one(1091629-60-5)
    11. EPA Substance Registry System: (S)-3-(fluorobis(phenylsulfonyl)methyl)-1-phenylpentan-1-one(1091629-60-5)

  • 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: 1091629-60-5(Hazardous Substances Data)

1091629-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1091629-60-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,1,6,2 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1091629-60:
(9*1)+(8*0)+(7*9)+(6*1)+(5*6)+(4*2)+(3*9)+(2*6)+(1*0)=155
155 % 10 = 5
So 1091629-60-5 is a valid CAS Registry Number.

1091629-60-5Downstream Products

1091629-60-5Relevant articles and documents

Catalytic enantioselective Michael addition of 1-fluoro-bis (phenylsulfonyl)methane to α,β-unsaturated ketones catalyzed by cinchona alkaloids

Furukawa, Tatsuya,Shibata, Norio,Mizuta, Satoshi,Nakamura, Shuichi,Toru, Takeshi,Shiro, Motoo

, p. 8051 - 8054 (2008)

(Chemical Equation Presented) A catalyst worth its salt: The ammonium salts of cinchona alkaloids possessing sterically demanding substituents effectively catalyzed the enantioselective 1,4-conjugate addition of 1-fluorobis(phenyl- sulfonyl) methane to α,β-unsaturated ketones to furnish the Michael adducts in high yield with excellent enantioselectivity (see scheme). The adducts are useful for the synthesis of chiral monofluoromethylated molecules.

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