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1338328-42-9

4,4,6,6,6-pentafluoro-5,5-dihydroxy-1-phenylhexan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1338328-42-9 Structure

  • Basic information

    1. Product Name: 4,4,6,6,6-pentafluoro-5,5-dihydroxy-1-phenylhexan-3-one
    2. Synonyms: 4,4,6,6,6-pentafluoro-5,5-dihydroxy-1-phenylhexan-3-one
    3. CAS NO:1338328-42-9
    4. Molecular Formula:
    5. Molecular Weight: 298.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338328-42-9.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: 4,4,6,6,6-pentafluoro-5,5-dihydroxy-1-phenylhexan-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,4,6,6,6-pentafluoro-5,5-dihydroxy-1-phenylhexan-3-one(1338328-42-9)
    11. EPA Substance Registry System: 4,4,6,6,6-pentafluoro-5,5-dihydroxy-1-phenylhexan-3-one(1338328-42-9)

  • 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: 1338328-42-9(Hazardous Substances Data)

1338328-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338328-42-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,3,2 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1338328-42:
(9*1)+(8*3)+(7*3)+(6*8)+(5*3)+(4*2)+(3*8)+(2*4)+(1*2)=159
159 % 10 = 9
So 1338328-42-9 is a valid CAS Registry Number.

1338328-42-9Relevant articles and documents

Synthesis of α-halo-α,α-difluoromethyl ketones by a trifluoroacetate release/halogenation protocol

John, Jinu P.,Colby, David A.

, p. 9163 - 9168 (2011/12/16)

Three series of α-halo-α,α-difluoromethyl ketones are prepared from highly α-fluorinated gem-diols by exploiting the facile release of trifluoroacetate, followed by immediate trapping of the liberated α,α-difluoroenolate with an electrophilic chlorine, br

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