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76580-08-0

1-(4-methoxyphenyl)-2-(naphthalen-1-yl)ethan-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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  • 76580-08-0 Structure

  • Basic information

    1. Product Name: 1-(4-methoxyphenyl)-2-(naphthalen-1-yl)ethan-1-one
    2. Synonyms: 1-(4-methoxyphenyl)-2-(naphthalen-1-yl)ethan-1-one
    3. CAS NO:76580-08-0
    4. Molecular Formula:
    5. Molecular Weight: 276.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76580-08-0.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: 1-(4-methoxyphenyl)-2-(naphthalen-1-yl)ethan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-methoxyphenyl)-2-(naphthalen-1-yl)ethan-1-one(76580-08-0)
    11. EPA Substance Registry System: 1-(4-methoxyphenyl)-2-(naphthalen-1-yl)ethan-1-one(76580-08-0)

  • 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: 76580-08-0(Hazardous Substances Data)

76580-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76580-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,8 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76580-08:
(7*7)+(6*6)+(5*5)+(4*8)+(3*0)+(2*0)+(1*8)=150
150 % 10 = 0
So 76580-08-0 is a valid CAS Registry Number.

76580-08-0Relevant articles and documents

Catalytic α-Arylation of Ketones with Heteroaromatic Esters

Isshiki, Ryota,Takise, Ryosuke,Itami, Kenichiro,Muto, Kei,Yamaguchi, Junichiro

supporting information, p. 2599 - 2603 (2017/10/31)

Heteroaromatic esters were found to be applicable as an arylating agent for the Pd-catalyzed α-arylation of ketones in a decarbonylative fashion. The use of our in-house ligand, dcypt, enabled this unique bond formation. Considering the ubiquity and low cost of aromatic esters, the present work will allow for rapid access to valuable α-aryl carbonyl compounds.

Selective Metal-Free Deoxygenation of Unsymmetrical 1,2-Dicarbonyl Compounds by Chlorotrimethylsilane and Sodium Iodide

Yuan, Ling-Zhi,Renko, Dolor,Khelifi, Ilhem,Provot, Olivier,Brion, Jean-Daniel,Hamze, Abdallah,Alami, Mouad

supporting information, p. 3238 - 3241 (2016/07/14)

For the first time, the combination of chlorotrimethylsilane with NaI is used as a selective reducting system toward 1,2-diketones. This combination is successfully evaluated with several unsymmetrically benzil derivatives, which are reduced in good yield

LIGAND, NICKEL COMPLEX COMPRISING LIGAND, AND REACTION USING NICKEL COMPLEX

-

Paragraph 0282; 0284; 0285, (2016/10/07)

PROBLEM TO BE SOLVED: To provide a method for directly carrying out arylation, especially α-arylation, of a carbonyl compound or a thiocarbonyl compound by using a more inexpensive phenol derivative and a nickel catalyst, and to provide a novel nickel cat

Nickel-catalyzed α-arylation of ketones with phenol derivatives

Takise, Ryosuke,Muto, Kei,Yamaguchi, Junichiro,Itami, Kenichiro

supporting information, p. 6791 - 6794 (2014/07/08)

The nickel-catalyzed α-arylation of ketones with readily available phenol derivatives (esters and carbamates) provides access to useful α-arylketones. For this transformation, 3,4-bis(dicyclohexylphosphino) thiophene (dcypt) was identified as a new, enabling, air-stable ligand for this transformation. The intermediate of an assumed C-O oxidative addition was isolated and characterized by X-ray crystal-structure analysis. The nickel-catalyzed α-arylation of ketones with readily available phenol derivatives (esters and carbamates) provides access to useful α-arylketones. The use of 3,4-bis(dicyclohexylphosphino)thiophene (dcypt) as an air-stable ligand enables this transformation. The intermediate of an assumed C-O oxidative addition was isolated and characterized by X-ray crystal-structure analysis.

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