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560080-39-9

2-(4-chlorophenyl)-N-(3,3-diphenylpropyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 560080-39-9 Structure

  • Basic information

    1. Product Name: 2-(4-chlorophenyl)-N-(3,3-diphenylpropyl)acetamide
    2. Synonyms: 2-(4-chlorophenyl)-N-(3,3-diphenylpropyl)acetamide
    3. CAS NO:560080-39-9
    4. Molecular Formula: C23H22ClNO
    5. Molecular Weight: 363.87988
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 560080-39-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-chlorophenyl)-N-(3,3-diphenylpropyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-chlorophenyl)-N-(3,3-diphenylpropyl)acetamide(560080-39-9)
    11. EPA Substance Registry System: 2-(4-chlorophenyl)-N-(3,3-diphenylpropyl)acetamide(560080-39-9)

  • 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: 560080-39-9(Hazardous Substances Data)

560080-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 560080-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,0,0,8 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 560080-39:
(8*5)+(7*6)+(6*0)+(5*0)+(4*8)+(3*0)+(2*3)+(1*9)=129
129 % 10 = 9
So 560080-39-9 is a valid CAS Registry Number.

560080-39-9Downstream Products

560080-39-9Relevant articles and documents

Triflic acid-mediated phenylation of N-acylaminoalkyl diethylacetals and N-acyl-2-phenyl cyclic amides

King, Frank D.,Caddick, Stephen

, p. 4361 - 4366 (2011/07/29)

The reaction of N-acylaminoalkyl diethylacetals with triflic acid in benzene gave N-acylamino-diphenylalkyls. The proposed intermediates are the N-acyl-2-phenyl cyclic amides, which themselves are similarly converted to N-acylamino-diphenylalkyls.

Acetamide derivatives with antioxidant activity and potential anti-inflammatory activity

Autore, Giuseppina,Caruso, Anna,Marzocco, Stefania,Nicolaus, Barbara,Palladino, Chiara,Pinto, Aldo,Popolo, Ada,Sinicropi, Maria S.,Tommonaro, Giuseppina,Saturnino, Carmela

experimental part, p. 2028 - 2038 (2010/06/13)

This study reports the synthesis and antioxidant activity of some new acetamide derivatives. The compounds' structures were elucidated by NMR analysis and their melting points were measured. The in vitro antioxidant activity of these compounds was tested

Novel sterically hindered cannabinoid CB1 receptor ligands

Urbani, Paolo,Cascio, Maria Grazia,Ramunno, Anna,Bisogno, Tiziana,Saturnino, Carmela,Marzo, Vincenzo Di

, p. 7510 - 7515 (2008/12/23)

In the present study, 11 novel N-(3,3-diphenyl)propyl-2,2-diphenylacetamide derivatives (4a-d and 9a-g) and six triphenylacetamides (10a-c and 11a-c) were synthesized and tested as ligands of cannabinoid CB1 and CB2 receptors. All co

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