Welcome to LookChem.com Sign In|Join Free
  • or
4-CHLORO-N-(2-FLUOROBENZYL)ANILINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

723753-84-2

Post Buying Request

723753-84-2 Suppliers

Recommended suppliers

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

723753-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 723753-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,3,7,5 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 723753-84:
(8*7)+(7*2)+(6*3)+(5*7)+(4*5)+(3*3)+(2*8)+(1*4)=172
172 % 10 = 2
So 723753-84-2 is a valid CAS Registry Number.

723753-84-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H56275)  4-Chloro-N-(2-fluorobenzyl)aniline, 97%   

  • 723753-84-2

  • 250mg

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H56275)  4-Chloro-N-(2-fluorobenzyl)aniline, 97%   

  • 723753-84-2

  • 1g

  • 4704.0CNY

  • Detail

723753-84-2Downstream Products

723753-84-2Relevant academic research and scientific papers

Switchable Bifunctional Bistate Reusable ZnO-Cu for Selective Oxidation and Reduction Reaction

Sarmah, Kasturi,Mukhopadhyay, Subhamoy,Maji, Tarun K.,Pratihar, Sanjay

, p. 732 - 745 (2019/01/11)

Herein we disclosed the utilization of copper loaded zinc oxide (ZnO-Cu) for its stimuli (O2/light) responsive switchable performance between its reduced (S-1) and oxidized (S-2) state for two antagonistic reactions, namely oxidation of alkyl arenes/heteroarenes to aldehydes/ketones and reduction of nitro arenes/heteroarenes to corresponding amines. The two states of the catalyst showed its switchable performance as highly active and poorly active catalyst for oxidation and reduction, and both reactions could be turned "off" and "on" by changing the stimuli (light and O2/N2). The switching efficiency between the states and their relative reactivity were found to be consistent under variety of reaction conditions and remain unaltered irrespective of oxidation-reduction (or vice versa) sequence and substrates used in the reaction. The photo catalysts (S-1 and S-2) demonstrated good catalytic activity, multiple reusability, broad substrate scope, and reasonable functional group tolerance for both the reactions and probed its quality performance in a large-scale setup. The system was used in an assisted tandem catalysis setup for the synthesis of benzyl amines utilizing both oxidation and reduction reaction by stimuli responsive switching between the states of the catalyst.

Selective reductive amination of aldehydes from nitro compounds catalyzed by molybdenum sulfide clusters

Pedrajas,Sorribes,Junge,Beller,Llusar

supporting information, p. 3764 - 3768 (2017/08/21)

Secondary amines are selectively obtained from low value starting materials using hydrogen and a non-noble metal-based catalyst. The reductive amination of aldehydes from nitroarenes or nitroalkanes is efficiently catalyzed by a well-defined diamino molybdenum sulfide cluster in a one-pot homogeneous reaction. The integrity of the molecular cluster catalyst is preserved along the process.

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 723753-84-2