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Acetic acid 4-acetyl-4-methyl-2-methylene-5-oxo-hexyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 196715-62-5 Structure
  • Basic information

    1. Product Name: Acetic acid 4-acetyl-4-methyl-2-methylene-5-oxo-hexyl ester
    2. Synonyms: Acetic acid 4-acetyl-4-methyl-2-methylene-5-oxo-hexyl ester
    3. CAS NO:196715-62-5
    4. Molecular Formula:
    5. Molecular Weight: 226.273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 196715-62-5.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: Acetic acid 4-acetyl-4-methyl-2-methylene-5-oxo-hexyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid 4-acetyl-4-methyl-2-methylene-5-oxo-hexyl ester(196715-62-5)
    11. EPA Substance Registry System: Acetic acid 4-acetyl-4-methyl-2-methylene-5-oxo-hexyl ester(196715-62-5)
  • 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: 196715-62-5(Hazardous Substances Data)

196715-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 196715-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,7,1 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 196715-62:
(8*1)+(7*9)+(6*6)+(5*7)+(4*1)+(3*5)+(2*6)+(1*2)=175
175 % 10 = 5
So 196715-62-5 is a valid CAS Registry Number.

196715-62-5Relevant articles and documents

Palladium-catalyzed annulation of monosubstituted β-diketones

Buono, Frédéric,Tenaglia, Alphonse

, p. 1153 - 1155 (2007/10/03)

Various 4-methylenecyclohexanones and bridged bicyclo[3.n.l]alkanones (n = 2 or 3) are readily available via a palladium-catalyzed C,C-dialkylative cyclisation of monoalkylated β-diketones with allylic diacetate 1a (or dicarbonate 1b). A one-pot bicycloannulation/retro Claisen fragmentation leading to medium-sized cycloalkanones from monoalkylated cyclic β-diketones is described.

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