Welcome to LookChem.com Sign In|Join Free

CAS

  • or

51786-73-3

Post Buying Request

51786-73-3 Suppliers

Recommended suppliersmore

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

51786-73-3 Usage

Description

1,10-Phenanthroline, 2,4,7,9-tetraphenylis a chemical compound that consists of a phenanthroline molecule connected to four phenyl rings. It is widely recognized for its chelating properties in coordination chemistry, enabling it to form complexes with various metal ions. 1,10-Phenanthroline, 2,4,7,9-tetraphenylis characterized by its unique structure and properties, which make it a versatile tool in different research fields, including chemical and biological research.

Uses

Used in Analytical Chemistry:
1,10-Phenanthroline, 2,4,7,9-tetraphenylis used as a reagent in spectrophotometric assays for the detection and quantification of metal ions. Its ability to form complexes with these ions allows for accurate and sensitive measurements, making it a valuable tool in analytical chemistry.
Used in Coordination Chemistry:
In the field of coordination chemistry, 1,10-Phenanthroline, 2,4,7,9-tetraphenylis used as a chelating agent to form coordination complexes with metal ions. These complexes are essential for studying the properties, structures, and reactivity of metal ions in various chemical systems.
Used in Organic Synthesis:
1,10-Phenanthroline, 2,4,7,9-tetraphenylis also utilized in organic synthesis for the preparation of coordination complexes. These complexes can be further modified or used as intermediates in the synthesis of more complex organic molecules.
Used in Bioinorganic Chemistry:
In the field of bioinorganic chemistry, 1,10-Phenanthroline, 2,4,7,9-tetraphenylis employed to study the roles and interactions of metal ions in biological systems. Its ability to form complexes with metal ions helps researchers understand the mechanisms and functions of these ions in biological processes.
Overall, 1,10-Phenanthroline, 2,4,7,9-tetraphenylis a versatile compound with a wide range of applications in various chemical and biological research fields, making it an essential tool for scientists and researchers.

Check Digit Verification of cas no

The CAS Registry Mumber 51786-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,8 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51786-73:
(7*5)+(6*1)+(5*7)+(4*8)+(3*6)+(2*7)+(1*3)=143
143 % 10 = 3
So 51786-73-3 is a valid CAS Registry Number.

51786-73-3Downstream Products

51786-73-3Relevant articles and documents

Copper-Catalyzed Reductive Trifluoromethylation of Alkyl Iodides with Togni's Reagent

Chen, Yanchi,Ma, Guobin,Gong, Hegui

, p. 4677 - 4680 (2018)

This work illustrates a reductive cross-electrophile coupling protocol for trifluoromethylation of alkyl iodides under Cu-catalyzed/Ni-promoted reaction conditions. The use of diboron esters as the terminal reductant allows the effective generation of the alkyl-CF3 products with excellent functional group tolerance and broad substrate scope. A mechanism involving a reaction of alkyl-Cu with Togni's reagent was proposed.

DIRECT SYNTHESIS OF DISUBSTITUTED AROMATIC POLYIMINE CHELATES

Dietrich-Buchecker, C. O.,Marnot, P. A.,Sauvage, J. P.

, p. 5291 - 5294 (2007/10/02)

The reaction of an alkyl- or aryl-lithium with 1,10-phenanthroline followed by hydrolysis and rearomatisation with manganese dioxide gives good yields of the 2,9-disubstituted product.This synthetic method has been extended to other polyimines such as 2,2'-bipyridine, 2,2',6',2''-terpyridine and 1,8-naphtyridine.

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

What can I do for you?
Get Best Price

Get Best Price for 51786-73-3