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109559-47-9

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109559-47-9 Usage

Description

1,10-Phenanthroline, 2-phenyl-, also known as Phenanthroline, is a chemical compound with the molecular formula C18H12N2. It is a heterocyclic compound consisting of two benzene rings fused to a phenanthroline core. 1,10-Phenanthroline, 2-phenylis known for its versatility as a ligand in coordination chemistry, often utilized in the synthesis of metal complexes. It also serves as a chelating agent and a fluorescent probe for metal ions. Due to its ability to form stable complexes with metal ions, 1,10-Phenanthroline, 2-phenylhas found applications in various fields such as biology, medicine, environmental science, and materials science.

Uses

Used in Coordination Chemistry:
1,10-Phenanthroline, 2-phenylis used as a versatile ligand in coordination chemistry for the synthesis of metal complexes. Its ability to form stable complexes with metal ions makes it a valuable compound in this field.
Used in Analytical Chemistry:
As a chelating agent, 1,10-Phenanthroline, 2-phenylis used in analytical chemistry for the detection and quantification of metal ions. Its interaction with metal ions allows for accurate measurements and analysis.
Used in Biology and Medicine:
1,10-Phenanthroline, 2-phenylis used as a fluorescent probe for metal ions in biological and medical applications. Its fluorescence properties enable the detection and monitoring of metal ion concentrations in various biological systems.
Used in Environmental Science:
In environmental science, 1,10-Phenanthroline, 2-phenylis used for the detection and analysis of metal ion contamination in various environmental samples, such as water, soil, and air.
Used in Materials Science:
1,10-Phenanthroline, 2-phenylis also utilized in materials science for the development of new materials with specific properties, such as metal-organic frameworks (MOFs) and coordination polymers, which can have applications in gas storage, catalysis, and drug delivery.

Check Digit Verification of cas no

The CAS Registry Mumber 109559-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,5 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109559-47:
(8*1)+(7*0)+(6*9)+(5*5)+(4*5)+(3*9)+(2*4)+(1*7)=149
149 % 10 = 9
So 109559-47-9 is a valid CAS Registry Number.

109559-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1,10-phenanthroline

1.2 Other means of identification

Product number -
Other names 2-Phenyl-[1,10]phenanthrolin

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:109559-47-9 SDS

109559-47-9Relevant articles and documents

A self-assembling receptor for dicarboxylic acids

Goodman, M. Scott,Weiss, Jean,Hamilton, Andrew D.

, p. 8943 - 8946 (1994)

In this paper we describe a simple binding subunit that self-assembles in the presence of metal ions to form a receptor for dicarboxylic acids. The resultant binding site is chiral and strong complexation to dicarboxylic acids in CDCl3 can be d

Nickel(II)-Catalyzed Asymmetric Michael Addition of Oxindoles with Modified N,N,O-Tridentate Chiral Phenanthroline Ligands

Naganawa, Yuki,Abe, Hiroki,Nishiyama, Hisao

supporting information, p. 1973 - 1978 (2016/08/09)

Nickel(II)-catalyzed enantioselective Michael addition of N-Boc-oxindole derivatives with methyl vinyl ketone was demonstrated to give the corresponding adducts having chiral all-carbon quaternary centers with up to 87% ee in the presence of axially chira

A rapid synthesis of asymmetric alkyl- and aryl-2,9-disubstitued 1,10-phenanthrolines

Jakobsen, S?ren,Tilset, Mats

experimental part, p. 3072 - 3074 (2011/06/23)

The finding that alkyl- and aryllithium reagents add almost instantly to the N-C2/C9 bond of 1,10-phenanthrolines led us to the development of a reaction scheme where the C2 and C9 positions of 1,10-phenanthroline can be functionalized by two different al

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