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426833-01-4

4-benzyloxy-2-methyl-1-phenylbutane-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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  • 426833-01-4 Structure

  • Basic information

    1. Product Name: 4-benzyloxy-2-methyl-1-phenylbutane-1,3-dione
    2. Synonyms: 4-benzyloxy-2-methyl-1-phenylbutane-1,3-dione
    3. CAS NO:426833-01-4
    4. Molecular Formula:
    5. Molecular Weight: 282.339
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 426833-01-4.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-benzyloxy-2-methyl-1-phenylbutane-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-benzyloxy-2-methyl-1-phenylbutane-1,3-dione(426833-01-4)
    11. EPA Substance Registry System: 4-benzyloxy-2-methyl-1-phenylbutane-1,3-dione(426833-01-4)

  • 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: 426833-01-4(Hazardous Substances Data)

426833-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 426833-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,6,8,3 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 426833-01:
(8*4)+(7*2)+(6*6)+(5*8)+(4*3)+(3*3)+(2*0)+(1*1)=144
144 % 10 = 4
So 426833-01-4 is a valid CAS Registry Number.

426833-01-4Relevant articles and documents

Enantioselective monoreduction of 2-alkyl 1,3-diketones using chiral ruthenium catalysts. Synthesis of the C14-C25 fragment of bafilomycin A 1

Eustache, Florence,Dalko, Peter I.,Cossy, Janine

, p. 8823 - 8826 (2007/10/03)

The enantioselective monoreduction of 2-alkyl 1,3-diketones by dynamic kinetic resolution using optically active ruthenium catalysts allowed the preparation of the C14-C25 fragment of bafilomycin A1.

Synthesis of the C14-C25 Subunit of Bafilomycin A1

Eustache, Florence,Dalko, Peter I.,Cossy, Janine

, p. 9994 - 10002 (2007/10/03)

The enantioselective synthesis of the C14-C25 subunit of bafilomycin A 1, was realized in a convergent route. The sequence involves two dynamic kinetic resolution steps of 2-alkyl 1,3-diketones that use optically active ruthenium complexes, an

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