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CAS

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133377-25-0

2,2-dimethoxy-1-phenyl-1-butanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133377-25-0 Structure

  • Basic information

    1. Product Name: 2,2-dimethoxy-1-phenyl-1-butanol
    2. Synonyms:
    3. CAS NO:133377-25-0
    4. Molecular Formula:
    5. Molecular Weight: 210.273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133377-25-0.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: 2,2-dimethoxy-1-phenyl-1-butanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dimethoxy-1-phenyl-1-butanol(133377-25-0)
    11. EPA Substance Registry System: 2,2-dimethoxy-1-phenyl-1-butanol(133377-25-0)

  • 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: 133377-25-0(Hazardous Substances Data)

133377-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133377-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,7 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 133377-25:
(8*1)+(7*3)+(6*3)+(5*3)+(4*7)+(3*7)+(2*2)+(1*5)=120
120 % 10 = 0
So 133377-25-0 is a valid CAS Registry Number.

133377-25-0Downstream Products

133377-25-0Relevant articles and documents

Electrochemical oxidation of ketones in methanol in the presence of alkali metal bromides

Nikishin, Gennady I.,Elinson, Michail N.,Makhova, Irina V.

, p. 895 - 905 (1991)

Electrochemical oxidation of methyl ketones in methanoi in the presence of alkali metal bromides affords methyl carboxylates. Benzyl alkyl ketones are transformed under similar conditions into methyl 3-phenylalkanoates, while ketones lacking σ-benzyl or σ-methyl group are oxidized into σ-hydroxyketals.

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