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5-Nitro-1,7-phenanthroline is an organic compound with the chemical formula C12H7N3O2. It is a derivative of phenanthroline, a heterocyclic aromatic compound, characterized by the presence of two nitrogen atoms in its structure. The "5-nitro" prefix indicates that there is a nitro group (-NO2) attached to the 5th carbon atom of the phenanthroline ring. 5-nitro-1,7-phenanthroline is often used as a reagent in analytical chemistry, particularly in the detection of metal ions such as iron and copper, due to its ability to form colored complexes with these ions. The nitro group in 5-nitro-1,7-phenanthroline enhances the sensitivity of the compound towards certain metal ions, making it a valuable tool in colorimetric assays and other analytical techniques.

41148-68-9

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41148-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41148-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,4 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41148-68:
(7*4)+(6*1)+(5*1)+(4*4)+(3*8)+(2*6)+(1*8)=99
99 % 10 = 9
So 41148-68-9 is a valid CAS Registry Number.

41148-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitro-1,7-phenanthroline

1.2 Other means of identification

Product number -
Other names 5-nitro-[1,7]phenanthroline

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:41148-68-9 SDS

41148-68-9Relevant academic research and scientific papers

Recyclable porous polymer-supported copper catalysts for Glaser and Huisgen 1,3-diolar cycloaddition reactions

Sun, Qi,Lv, Zhonfei,Du, Yuyang,Wu, Qinming,Wang, Liang,Zhu, Longfeng,Meng, Xiangju,Chen, Wanzhi,Xiao, Feng-Shou

supporting information, p. 2822 - 2827 (2013/11/19)

A family of polymer-attached phenanthrolines was prepared from solvothermal copolymerization of divinylbenzene with N-(1,10-phenanthroline-5-yl)acrylamide in different ratios. The polymer-supported copper catalysts were obtained through typical impregnation with copper(II) salts. The polymers and supported copper catalysts have been characterized by N2 adsortion, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermogravimetric analysis (TG); they exhibit a high surface area, hierarchical porosity, large pore volume, and high thermal and chemical stabilities. The copper catalyst has proved to be highly active for Glaser homocoupling of alkynes and Huisgen 1,3-diolar cycloaddition of alkynes with benzyl azide under mild conditions at low catalyst loading. The heterogeneous copper catalyst is more active than commonly used homogeneous and nonporous polystyrene-supported copper catalysts. In particular, the catalyst is easily recovered and can be recycled at least ten times without any obvious loss in catalytic activity. Metal leaching was prevented due to the strong binding ability of phenanthroline and products were not contaminated with copper, as determined by ICP analysis. At the Copper, Coppercabana: Stable, porous polymer-attached phenanthrolines were successfully prepared from solvothermal copolymerization of divinylbenzene with N-(1,10-phenanthrolin-5-yl)acrylamide (PCP-Phen). After coordination with copper species, a heterogeneous copper catalyst was obtained that displayed a higher activity in Glaser and Huisgen couplings than commonly used homogeneous and nonporous polystyrene-supported copper catalysts. The copper catalyst has excellent recyclability due to the strong coordination ability of phenanthrolines. Copyright

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