Welcome to LookChem.com Sign In|Join Free
  • or
6-Ethoxy-2-phenylquinoline is a chemical compound with the molecular formula C17H15NO. It is a derivative of quinoline, a heterocyclic aromatic organic compound with a benzene ring fused to a pyridine ring. The presence of an ethoxy group at the 6-position and a phenyl group at the 2-position distinguishes it from other quinoline derivatives. 6-ethoxy-2-phenylquinoline is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of dyes and pigments. Its chemical structure and properties make it a versatile building block in organic synthesis, particularly in the development of new compounds with specific biological activities.

4789-74-6

Post Buying Request

4789-74-6 Suppliers

Recommended suppliers

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

4789-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4789-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,8 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4789-74:
(6*4)+(5*7)+(4*8)+(3*9)+(2*7)+(1*4)=136
136 % 10 = 6
So 4789-74-6 is a valid CAS Registry Number.

4789-74-6Relevant academic research and scientific papers

An Unexpected Construction of 2-Arylquinolines from N-Cinnamylanilines through sp3 Ci-H Aerobic Oxidation Induced by a Catalytic Radical Cation Salt

Liu, Fang,Yu, Liangliang,Lv, Shiwei,Yao, Junjun,Liu, Jing,Jia, Xiaodong

, p. 459 - 465 (2016)

An unexpected reaction of cinnamylanilines was achieved through the radical cation salt-induced aerobic oxidation of sp3 C-H bonds, providing a series of 2-arylquinolines. The mechanistic study shows that the cinnamylaniline was oxidized to an imine, which was attacked by the aniline generated through decomposition of the corresponding imine. After further intramolecular cyclization and aromatization, 2-arylquinolines were obtained. This reaction provides a new method to construct 2-arylquinolines from readily accessible starting materials.

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 4789-74-6