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3,3-dimethoxy-2-phenyl-propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 59845-64-6 Structure
  • Basic information

    1. Product Name: 3,3-dimethoxy-2-phenyl-propionic acid methyl ester
    2. Synonyms:
    3. CAS NO:59845-64-6
    4. Molecular Formula:
    5. Molecular Weight: 224.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59845-64-6.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: 3,3-dimethoxy-2-phenyl-propionic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3-dimethoxy-2-phenyl-propionic acid methyl ester(59845-64-6)
    11. EPA Substance Registry System: 3,3-dimethoxy-2-phenyl-propionic acid methyl ester(59845-64-6)
  • 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: 59845-64-6(Hazardous Substances Data)

59845-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59845-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,4 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59845-64:
(7*5)+(6*9)+(5*8)+(4*4)+(3*5)+(2*6)+(1*4)=176
176 % 10 = 6
So 59845-64-6 is a valid CAS Registry Number.

59845-64-6Downstream Products

59845-64-6Relevant articles and documents

Novel α-Formylation of α,α-Disubstituted Esters. Trimethylsilyl Trifluoromethanesulfonate-catalysed Reaction of Ketene Silyl Acetals with N-t-Butylformimidoyl Cyanide

Okano, Kohji,Morimoto, Toshiaki,Sekiya, Minoru

, p. 119 - 120 (1985)

General α-formylation of α,α-disubstituted methyl acetates can be achieved by the reaction of ketene silyl acetals (1) with N-t-butylformimidoyl cyanide (2) in the presence of trimethylsilyl trifluoromethanesulphonate (3) as catalyst followed by hydrolysi

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