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2-Isopropenyl-5-methyl-6-phenyl-6-piperidin-1-yl-6H-[1,3]oxazin-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148932-11-0 Structure
  • Basic information

    1. Product Name: 2-Isopropenyl-5-methyl-6-phenyl-6-piperidin-1-yl-6H-[1,3]oxazin-4-ol
    2. Synonyms: 2-Isopropenyl-5-methyl-6-phenyl-6-piperidin-1-yl-6H-[1,3]oxazin-4-ol
    3. CAS NO:148932-11-0
    4. Molecular Formula:
    5. Molecular Weight: 312.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148932-11-0.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-Isopropenyl-5-methyl-6-phenyl-6-piperidin-1-yl-6H-[1,3]oxazin-4-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Isopropenyl-5-methyl-6-phenyl-6-piperidin-1-yl-6H-[1,3]oxazin-4-ol(148932-11-0)
    11. EPA Substance Registry System: 2-Isopropenyl-5-methyl-6-phenyl-6-piperidin-1-yl-6H-[1,3]oxazin-4-ol(148932-11-0)
  • 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: 148932-11-0(Hazardous Substances Data)

148932-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148932-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,3 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 148932-11:
(8*1)+(7*4)+(6*8)+(5*9)+(4*3)+(3*2)+(2*1)+(1*1)=150
150 % 10 = 0
So 148932-11-0 is a valid CAS Registry Number.

148932-11-0Downstream Products

148932-11-0Relevant articles and documents

Novel Cycloaddition Reactions of Methacryloyl Isocyanate with Enamines

Tsuge, Otohiko,Hatta, Taizo,Mizuguchi, Ryuzo,Kato, Hisayoshi

, p. 631 - 634 (1993)

Methacryloyl isocyanate (MAI) functioned as an ambident heterodiene in the cycloaddition reactions. Thus, enamines added not only to the acyl isocyanato moiety, but also to the enone moiety in MAI. Regiochemistry of this cycloaddition markedly depended on the reaction conditions. The pathways for the formation of products are also described.

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