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1020038-85-0

1-(3,5-dimethylphenyl)butane-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1020038-85-0 Structure

  • Basic information

    1. Product Name: 1-(3,5-dimethylphenyl)butane-1,3-dione
    2. Synonyms: 1-(3,5-dimethylphenyl)butane-1,3-dione
    3. CAS NO:1020038-85-0
    4. Molecular Formula:
    5. Molecular Weight: 190.242
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1020038-85-0.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: 1-(3,5-dimethylphenyl)butane-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3,5-dimethylphenyl)butane-1,3-dione(1020038-85-0)
    11. EPA Substance Registry System: 1-(3,5-dimethylphenyl)butane-1,3-dione(1020038-85-0)

  • 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: 1020038-85-0(Hazardous Substances Data)

1020038-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1020038-85-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,0,3 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1020038-85:
(9*1)+(8*0)+(7*2)+(6*0)+(5*0)+(4*3)+(3*8)+(2*8)+(1*5)=80
80 % 10 = 0
So 1020038-85-0 is a valid CAS Registry Number.

1020038-85-0Downstream Products

1020038-85-0Relevant articles and documents

Palladium-catalysed carbonylative α-arylation of acetone and acetophenones to 1,3-diketones

Schranck, Johannes,Tlili, Anis,Alsabeh, Pamela G.,Neumann, Helfried,Stradiotto, Mark,Beller, Matthias

, p. 12624 - 12628 (2013)

Three COmponent α-arylation: A carbonylative ketone α-arylation process employing acetone for the first time, as well as acetophenones, is described (see scheme). The reaction tolerates a range of (hetero)aryl iodides and several functionalised aryl ketone coupling partners. Only low pressures of molecular CO are applied and no additional solvent is necessary. Copyright

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