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CAS

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1380396-97-3

ethyl (2E)-5-benzoyl-2-methyl-4-(1-naphthyl)-6-oxo-6-phenylhex-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1380396-97-3 Structure

  • Basic information

    1. Product Name: ethyl (2E)-5-benzoyl-2-methyl-4-(1-naphthyl)-6-oxo-6-phenylhex-2-enoate
    2. Synonyms:
    3. CAS NO:1380396-97-3
    4. Molecular Formula:
    5. Molecular Weight: 476.572
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380396-97-3.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: ethyl (2E)-5-benzoyl-2-methyl-4-(1-naphthyl)-6-oxo-6-phenylhex-2-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (2E)-5-benzoyl-2-methyl-4-(1-naphthyl)-6-oxo-6-phenylhex-2-enoate(1380396-97-3)
    11. EPA Substance Registry System: ethyl (2E)-5-benzoyl-2-methyl-4-(1-naphthyl)-6-oxo-6-phenylhex-2-enoate(1380396-97-3)

  • 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: 1380396-97-3(Hazardous Substances Data)

1380396-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380396-97-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,3,9 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1380396-97:
(9*1)+(8*3)+(7*8)+(6*0)+(5*3)+(4*9)+(3*6)+(2*9)+(1*7)=183
183 % 10 = 3
So 1380396-97-3 is a valid CAS Registry Number.

1380396-97-3Downstream Products

1380396-97-3Relevant articles and documents

Controlled reactions of 2,3-allenoates with a 1,3-diketone catalyst effect

Fang, Zhao,Fu, Chunling,Ma, Shengming

, p. 2585 - 2596 (2012)

Two types of reactions of 2,3-allenoates with 1,3-diketones under different reaction conditions are described: under palladium catalysis, the relatively electron-rich C=C bonds are attacked to afford ethyl (2E)-4-acyl-2-alkyl-4-aryl- 6-oxohept-2-enoates exclusively with dicyclohexyl(2,4,6-trimethoxyphenyl) phosphane as the ligand; under Cu(OAc)2 catalysis, 4-[R-C(=O)-]-(LB-Phos) 3,5-dialkyl-3-(2-oxo-2-arylethyl)furan-2(3H)-one products are formed unexpectedly through intramolecular reaction at the electron-deficient C=C bond.

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