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1,10-Phenanthroline, 5,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182319-03-5

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182319-03-5 Usage

Explanation

1,10-Phenanthroline, 5,6-diphenylis a derivative of the heterocyclic compound 1,10-phenanthroline, which means it is structurally similar but has additional functional groups or modifications.
3. Heterocyclic Compound

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, hydrogen, and nitrogen.
4. Chelating Ligand

Explanation

1,10-Phenanthroline, 5,6-diphenylis used as a chelating ligand in coordination chemistry, meaning it can form multiple bonds with a central metal ion, creating a stable complex.
5. Diphenyl Substitution

Explanation

The molecule has two phenyl groups (C6H5) attached to the 5 and 6 positions of the phenanthroline ring, which adds aromaticity and bulkiness to the molecule.
6. Aromaticity

Explanation

The presence of diphenyl groups in the molecule contributes to its aromaticity, which is the property of being stable and having a characteristic smell due to the presence of unsaturated cyclic structures.
7. Bulkiness

Explanation

The diphenyl substitution increases the size and steric hindrance of the molecule, which can affect its chemical properties and interactions with other molecules.
8. Potential Applications

Explanation

1,10-Phenanthroline, 5,6-diphenylhas been studied for its potential applications in various fields, including materials science, pharmaceuticals, and organic synthesis.
9. Biological Activities

Explanation

The compound may exhibit biological activities that are of interest for medicinal chemistry research, suggesting that it could have potential therapeutic or diagnostic applications.
10. Coordination Chemistry

Explanation

The study of how metal ions interact with ligands, such as 1,10-Phenanthroline, 5,6-diphenyl-, to form coordination complexes, which can have unique properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 182319-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,1 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 182319-03:
(8*1)+(7*8)+(6*2)+(5*3)+(4*1)+(3*9)+(2*0)+(1*3)=125
125 % 10 = 5
So 182319-03-5 is a valid CAS Registry Number.

182319-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-diphenyl-1,10-phenanthroline

1.2 Other means of identification

Product number -
Other names 1,10-Phenanthroline,5,6-diphenyl

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:182319-03-5 SDS

182319-03-5Relevant articles and documents

Rhodium(III)-Catalyzed Oxidative Annulation of 2,2′-Bipyridine N-Oxides with Alkynes via Dual C-H Bond Activation

Xu, Xin,Zhao, Haoqiang,Xu, Jianbin,Chen, Changjun,Pan, Yixiao,Luo, Zhenli,Zhang, Zongyao,Li, Huanrong,Xu, Lijin

supporting information, p. 3843 - 3847 (2018/07/25)

Rh(III)-catalyzed switchable annulation of 2,2′-bipyridine N-oxides with internal alkynes via dual C-H bond activation has been developed. Tuning the reaction conditions enabled the reaction pathway to be switched between rollover and nonrollover annulation, delivering 5,6-disubstituted-1,10-phenanthrolines and 5,6,7,8-tetrasubstituted-1-(pyridin-2-yl)isoquinoline 2-oxides in high yields, respectively. The procedures feature excellent regioselectivity, broad substrate scope, and high tolerance of functional groups. The synthetic utilities of these obtained products were demonstrated in the catalytic reactions.

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