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(E)-4-(2-(p-methoxybenzoylmethylene)phenyl)-3-buten-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415033-57-6 Structure
  • Basic information

    1. Product Name: (E)-4-(2-(p-methoxybenzoylmethylene)phenyl)-3-buten-2-one
    2. Synonyms: (E)-4-(2-(p-methoxybenzoylmethylene)phenyl)-3-buten-2-one
    3. CAS NO:1415033-57-6
    4. Molecular Formula:
    5. Molecular Weight: 294.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415033-57-6.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-(2-(p-methoxybenzoylmethylene)phenyl)-3-buten-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-(2-(p-methoxybenzoylmethylene)phenyl)-3-buten-2-one(1415033-57-6)
    11. EPA Substance Registry System: (E)-4-(2-(p-methoxybenzoylmethylene)phenyl)-3-buten-2-one(1415033-57-6)
  • 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: 1415033-57-6(Hazardous Substances Data)

1415033-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415033-57-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,0,3 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1415033-57:
(9*1)+(8*4)+(7*1)+(6*5)+(5*0)+(4*3)+(3*3)+(2*5)+(1*7)=116
116 % 10 = 6
So 1415033-57-6 is a valid CAS Registry Number.

1415033-57-6Downstream Products

1415033-57-6Relevant articles and documents

NHC Bronsted base-catalyzed transformations of isochromene derivatives: Regulation of products by the structures of carbene catalysts

Fan, Xing-Wen,Cheng, Ying

, p. 9079 - 9084,6 (2020/10/15)

Two different transformations of α-(isochromen-1-yl)ketones catalyzed by NHC Bronsted bases are reported. In the presence of a triazole carbene, α-(isochromen-1-yl)ketones isomerized into β-(2-(aroylmethylene) phenyl)-α,β-unsaturated ketones in 38-88% yields, while the same reaction catalyzed by an imidazole carbene produced 1-aroylnaphthalene derivatives in 90-99% yields. This work not only provides a new method for the synthesis of a novel type of α,β-unsaturated ketone and multi-substituted naphthalene derivatives, but also advances the application of NHC catalysts in the field of Bronsted base-catalysis.

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