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CAS

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83181-24-2

(E)-4-Methyl-5-oxo-5-phenyl-pent-2-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83181-24-2 Structure

  • Basic information

    1. Product Name: (E)-4-Methyl-5-oxo-5-phenyl-pent-2-enal
    2. Synonyms:
    3. CAS NO:83181-24-2
    4. Molecular Formula:
    5. Molecular Weight: 188.226
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83181-24-2.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: (E)-4-Methyl-5-oxo-5-phenyl-pent-2-enal(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-Methyl-5-oxo-5-phenyl-pent-2-enal(83181-24-2)
    11. EPA Substance Registry System: (E)-4-Methyl-5-oxo-5-phenyl-pent-2-enal(83181-24-2)

  • 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: 83181-24-2(Hazardous Substances Data)

83181-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83181-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,8 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83181-24:
(7*8)+(6*3)+(5*1)+(4*8)+(3*1)+(2*2)+(1*4)=122
122 % 10 = 2
So 83181-24-2 is a valid CAS Registry Number.

83181-24-2Downstream Products

83181-24-2Relevant articles and documents

O-SILYLATED ENOLATE PHENYLTHIOALKYLATION: A NEW SYNTHESIS OF UNSATURATED 1,5-DICARBONYL COMPOUNDS.

Khan, Hassan A.,Paterson, Ian

, p. 2399 - 2402 (1982)

The O-silylated enolates of ketones and esters can be phenylthioalkylated by the chlorides (2) and (3) under ZnBr2-catalysis; ozonolysis and subsequent sulphoxide thermolysis then gives the corresponding unsaturated 1,5-dicarbonyl compounds.

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