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1,10-Phenanthroline, 3-phenylis an organic compound characterized by a phenanthroline core with a phenyl group attached at the 3-position. 1,10-Phenanthroline, 3-phenylis recognized for its ability to form complexes with metal ions, especially transition metals, and has found applications in various scientific fields such as biochemistry, analytical chemistry, and material science. Its unique properties and reactivity also make it a valuable component in the synthesis of diverse molecular structures and materials.

110746-01-5

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110746-01-5 Usage

Uses

Used in Coordination Chemistry:
1,10-Phenanthroline, 3-phenylis used as a chelating ligand for forming complexes with metal ions, particularly transition metals. This application is crucial in coordination chemistry, where understanding the interactions between metal ions and organic ligands is essential for developing new materials and catalysts.
Used in Biochemistry:
In the field of biochemistry, 1,10-Phenanthroline, 3-phenylis utilized for studying the role of metal ions in biological systems. Its ability to complex with metal ions allows researchers to investigate the function and mechanisms of metalloenzymes and metalloproteins.
Used in Analytical Chemistry:
1,10-Phenanthroline, 3-phenylis employed as a reagent in analytical chemistry for the detection and quantification of metal ions. Its selective complexation with certain metals makes it a valuable tool for developing sensitive and specific analytical methods.
Used in Material Science:
In material science, 1,10-Phenanthroline, 3-phenylis used as a building block in the synthesis of new materials with unique properties. Its ability to form complexes with metal ions can lead to the development of materials with enhanced electrical, magnetic, or optical characteristics.
Used in Catalysis:
1,10-Phenanthroline, 3-phenylhas been investigated for its potential applications in catalysis, where it can be used to modify the properties of catalysts or to create new catalytic systems. Its interaction with metal ions can enhance the catalytic activity and selectivity of these systems.
Used in Sensing:
1,10-Phenanthroline, 3-phenylis also explored for its use in sensing applications, where its ability to form complexes with metal ions can be exploited to develop sensors with high sensitivity and selectivity for detecting specific metal ions in various environments.
Used in Medical Research:
1,10-Phenanthroline, 3-phenylis being investigated for its potential applications in medical research, particularly in the development of new drugs and therapies. Its interaction with metal ions may provide insights into the mechanisms of various diseases and contribute to the design of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 110746-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,7,4 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110746-01:
(8*1)+(7*1)+(6*0)+(5*7)+(4*4)+(3*6)+(2*0)+(1*1)=85
85 % 10 = 5
So 110746-01-5 is a valid CAS Registry Number.

110746-01-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-1,10-phenanthroline

1.2 Other means of identification

Product number -
Other names 1,10-Phenanthroline,3-phenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:110746-01-5 SDS

110746-01-5Downstream Products

110746-01-5Relevant academic research and scientific papers

Chelation-assisted electrocyclic reactions of 3-alkenyl-2,2′- bipyridines: An efficient method for the synthesis of 5,6-dihydro-1,10- phenanthroline and 1,10-phenanthroline derivatives

Takahashi, Akihiko,Hirose, Yuko,Kusama, Hiroyuki,Iwasawa, Nobuharu

, p. 609 - 611 (2008/09/20)

An efficient method for the synthesis of substituted 5,6-dihydro-1,10- phenanthrolines and 1,10-phenanthrolines has been developed by means of the chelation-assisted photochemical electrocyclic reactions of 3-alkenyl-2, 2′-bipyridines. The Royal Society o

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