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105243-57-0

2-(3,5-dimethoxyphenoxy)-1-phenylethan-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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  • 105243-57-0 Structure

  • Basic information

    1. Product Name: 2-(3,5-dimethoxyphenoxy)-1-phenylethan-1-one
    2. Synonyms: 2-(3,5-dimethoxyphenoxy)-1-phenylethan-1-one
    3. CAS NO:105243-57-0
    4. Molecular Formula:
    5. Molecular Weight: 272.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105243-57-0.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-(3,5-dimethoxyphenoxy)-1-phenylethan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3,5-dimethoxyphenoxy)-1-phenylethan-1-one(105243-57-0)
    11. EPA Substance Registry System: 2-(3,5-dimethoxyphenoxy)-1-phenylethan-1-one(105243-57-0)

  • 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: 105243-57-0(Hazardous Substances Data)

105243-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105243-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,4 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105243-57:
(8*1)+(7*0)+(6*5)+(5*2)+(4*4)+(3*3)+(2*5)+(1*7)=90
90 % 10 = 0
So 105243-57-0 is a valid CAS Registry Number.

105243-57-0Relevant articles and documents

Efficient synthetic approach to substituted benzo[b]furans and benzo[b]thiophenes by iodine-promoted cyclization of enaminones

Labarrios, Ehecatl,Jerezano, Alberto,Jimenez, Fabiola,Del Carmen Cruz, Maria,Delgado, Francisco,Zepeda, L. Gerardo,Tamariz, Joaquin

, p. 954 - 971 (2014/08/05)

An efficient synthetic approach to the substituted benzo[b]furan and benzo[b]thiophene scaffolds by iodine-mediated cyclization of the corresponding enaminones is described. This protocol was applied to a large series of these latter precursors to afford the respective benzoheterocycles substituted at the C-2 position by a carbonyl group functionality. A study of the factors that control this process reveals that the reactivity depends on the presence of electron-donor groups in the aryl ring of the aryloxycarbonylic and arylthiocarbonylic moieties.

A new synthetic route of 2-aroyl- and 2-benzyl-benzofurans and their application in the total synthesis of a metabolite isolated from dorstenia gigas

Correa, Christian,Cruz, Maria Del Carmen,Jimnez, Fabiola,Zepeda, L. Gerardo,Tamariz, Joaqun

experimental part, p. 991 - 999 (2009/04/06)

The Lewis acid-catalyzed cyclization of the (Z)-3-(dimethylamino)-2- aryloxy-1-arylprop-2-en-1-ones 4ah leads to a regioselective and short synthesis of 2-aroylbenzofurans 2ah. The WolffKishner reduction of the latter yielded a series of substituted 2-ben

Preparation of activated benzofurans and their reactions with aldehydes

Black, David St.C.,Craig, Donald C.,Kumar, Naresh,Rezaie, Robert

, p. 4803 - 4814 (2007/10/03)

Reactions of 3-substituted 4,6-dimethoxybenzofurans with formaldehyde and aryl aldeydes in the presence of acetic acid and phosphoryl chloride respectively give new macrocyclic calix[3]benzofurans, predominantly with an unsymmetrical linkage pattern. Inco

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