Welcome to LookChem.com Sign In|Join Free
  • or
1,4-Diphenylpyrrolidin-2-one is a chemical compound with the molecular formula C17H17NO. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 1,4-diphenylpyrrolidin-2-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure. It serves as an important intermediate in the preparation of certain drugs, particularly those with analgesic and anti-inflammatory properties. The compound's structure, which includes a pyrrolidinone ring fused to two phenyl groups, contributes to its reactivity and utility in organic synthesis. It is also of interest to researchers for its potential role in the development of new materials and compounds with specific therapeutic or chemical properties.

2889-64-7

Post Buying Request

2889-64-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2889-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2889-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2889-64:
(6*2)+(5*8)+(4*8)+(3*9)+(2*6)+(1*4)=127
127 % 10 = 7
So 2889-64-7 is a valid CAS Registry Number.

2889-64-7Downstream Products

2889-64-7Relevant academic research and scientific papers

Catalytic N-Alkylation of Amines Using Carboxylic Acids and Molecular Hydrogen

Sorribes, Iván,Cabrero-Antonino, Jose R.,Vicent, Cristian,Junge, Kathrin,Beller, Matthias

, p. 13580 - 13587 (2015)

A convenient, practical and green N-alkylation of amines has been accomplished by applying readily available carboxylic acids in the presence of molecular hydrogen. Applying an in situ formed ruthenium/triphos complex and an organic acid as cocatalyst, a broad range of alkylated secondary and tertiary amines are obtained in good to excellent yields. This novel method is also successfully applied for the synthesis of unsymmetrically substituted N-methyl/alkyl anilines through a direct three-component coupling reaction of the corresponding amines, carboxylic acids, and CO2 as a C1 source.

Synthesis of Pyrrolidines and Pyrrolizidines with α-Pseudoquaternary Centers by Copper-Catalyzed Condensation of α-Diazodicarbonyl Compounds and Aryl γ-Lactams

Goudedranche, Sébastien,Besnard, Céline,Egger, Léo,Lacour, Jér?me

, p. 13775 - 13779 (2016)

N-aryl γ-lactams react intermolecularly with acceptor–acceptor diazo reagents, usually dicarbonyl compounds, in a copper-catalyzed process to yield functionalized pyrrolidines with α-pseudoquaternary centers. As 1,2-acyl or -phosphoryl migration is prefer

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2889-64-7