Welcome to LookChem.com Sign In|Join Free
  • or
Quinoline, 3-bromo-2-phenyl-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61831-14-9

Post Buying Request

61831-14-9 Suppliers

Recommended suppliers

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

61831-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61831-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,3 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61831-14:
(7*6)+(6*1)+(5*8)+(4*3)+(3*1)+(2*1)+(1*4)=109
109 % 10 = 9
So 61831-14-9 is a valid CAS Registry Number.

61831-14-9Downstream Products

61831-14-9Relevant academic research and scientific papers

Visible-light-promoted c2 selective arylation of quinoline and pyridine n-oxides with diaryliodonium tetrafluoroborate

Li, Dazhi,Liang, Ce,Jiang, Zaixing,Zhang, Junzheng,Zhuo, Wang-Tao,Zou, Fan-Yue,Wang, Wan-Peng,Gao, Guo-Lin,Song, Jinzhu

, p. 2733 - 2742 (2020/03/11)

A protocol of visible-light-promoted C2 selective arylation of quinoline and pyridine N-oxides, with diaryliodonium tetrafluoroborate as an arylation reagent, using eosin Y as a photocatalyst for the construction of N-heterobiaryls was presented. This met

Preparation method of 2- aryl substituted quinoline nitrogen oxide compound

-

Paragraph 0067-0077, (2020/03/16)

The preparation method 2 - of, aryl-substituted quinoline nitrogen oxide is 2 - The method, according to the present invention provides,aryl-substituted quinoline nitrogen oxide compound, in a nitrogen atmosphere at room temperature, The method for prepar

KMnO4-mediated direct selective radical cross-coupling: An effective strategy for C2 arylation of quinoline N-oxide with arylboronic acids

Yuan, Jin-Wei,Qu, Ling-Bo

supporting information, p. 981 - 985 (2017/05/22)

Direct C[sbnd]H functionalization of quinoline N-oxides with arylboronic acids is achieved using KMnO4 as the sole and efficient oxidative system. This method provides an efficient protocol to construct regioselectively 2-arylquinoline N-oxides

Chemoselective synthesis of quinoline N-oxides from 3-(2-nitrophenyl)-3- hydroxypropanones

Okuma, Kentaro,Seto, Jun-Ichi,Nagahora, Noriyoshi,Shioji, Kosei

experimental part, p. 1372 - 1378 (2011/01/05)

The reaction of 3-(2-nitrophenyl)-3-hydroxypropanones with Zn/NH 4Cl gave the corresponding quinoline N-oxides in 80-90% yields. The reaction initiated the reduction of nitro group to afford the corresponding hydroxylamine, which intramolecularly condensed and followed by dehydration to give quinoline N-oxide. Although treatment of 2-nitrochalcone with Zn/NH 4Cl in EtOH/H2O resulted in the formation of quinoline N-oxide in low yield, the reaction of 2-nitrochalcone with Sn/NH4Cl in refluxing EtOH/H2O afforded quinoline N-oxide in 80% yield.

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 61831-14-9