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1220971-92-5

1-phenyldeca-2,3-dien-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1220971-92-5 Structure

  • Basic information

    1. Product Name: 1-phenyldeca-2,3-dien-1-one
    2. Synonyms: 1-phenyldeca-2,3-dien-1-one
    3. CAS NO:1220971-92-5
    4. Molecular Formula:
    5. Molecular Weight: 228.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1220971-92-5.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-phenyldeca-2,3-dien-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyldeca-2,3-dien-1-one(1220971-92-5)
    11. EPA Substance Registry System: 1-phenyldeca-2,3-dien-1-one(1220971-92-5)

  • 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: 1220971-92-5(Hazardous Substances Data)

1220971-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1220971-92-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,0,9,7 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1220971-92:
(9*1)+(8*2)+(7*2)+(6*0)+(5*9)+(4*7)+(3*1)+(2*9)+(1*2)=135
135 % 10 = 5
So 1220971-92-5 is a valid CAS Registry Number.

1220971-92-5Downstream Products

1220971-92-5Relevant articles and documents

Synthesis of 3-Keto Pyridines from the Conjugated Allenone – Alkynylamine Oxidative Cyclization Catalyzed by Supported Au Nanoparticles

Fragkiadakis, Michael,Kidonakis, Marios,Stratakis, Manolis,Zorba, Leandros

, p. 964 - 968 (2020)

Recyclable supported Au nanoparticles on TiO2 catalyze the cyclization of N-propargyl or N-homopropargyl β-enaminones followed by dehydrogenation (aromatization) leading to substituted 3-keto pyridines or 4-picolines in very good yields. This pathway is in contrast to their known cyclization in the presence of Au(I) or Au(III) catalysts which provides 1,4-oxazepines, instead. The enaminones are formed in situ upon mixing a conjugated allenone or allenyl ester with the alkynylamine, thus the pyridine-forming transformation is typically a one pot process. (Figure presented.).

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