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1,10-Phenanthroline, 2,9-dichloro-4,7-diphenylis a chemical compound that serves as a chelating ligand for metal ions. It is characterized by its high affinity for transition metals such as copper, iron, and ruthenium. 1,10-Phenanthroline, 2,9-dichloro-4,7-diphenylis widely used in chemical and biochemical research for the detection and quantification of various metal ions. Its unique chemical structure and diverse properties make it a valuable tool in scientific disciplines, including its potential biological activities as an anticancer agent and enzyme inhibitor.

1229012-68-3

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1229012-68-3 Usage

Uses

Used in Chemical and Biochemical Research:
1,10-Phenanthroline, 2,9-dichloro-4,7-diphenylis used as a chelating ligand for metal ions in chemical and biochemical research. Its high affinity for transition metals makes it an effective reagent for the detection and quantification of these metal ions.
Used in Analytical Applications:
In analytical chemistry, 1,10-Phenanthroline, 2,9-dichloro-4,7-diphenylis used as a reagent for the analysis of metal ions. Its ability to form complexes with transition metals allows for the accurate determination of metal concentrations in various samples.
Used in Synthetic Applications:
1,10-Phenanthroline, 2,9-dichloro-4,7-diphenylis also utilized in synthetic chemistry for the preparation of metal complexes. Its strong binding to metal ions facilitates the synthesis of new compounds with potential applications in various fields.
Used in Anticancer Applications:
1,10-Phenanthroline, 2,9-dichloro-4,7-diphenylhas been studied for its potential as an anticancer agent. Its ability to interact with metal ions and inhibit certain enzymes may contribute to its anticancer properties, making it a promising candidate for further research and development in cancer therapy.
Used in Enzyme Inhibition:
1,10-Phenanthroline, 2,9-dichloro-4,7-diphenylhas been found to inhibit certain enzymes, which may have implications in various biological processes. Its enzyme-inhibiting properties can be explored for potential therapeutic applications in treating diseases related to enzyme dysregulation.

Check Digit Verification of cas no

The CAS Registry Mumber 1229012-68-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,0,1 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1229012-68:
(9*1)+(8*2)+(7*2)+(6*9)+(5*0)+(4*1)+(3*2)+(2*6)+(1*8)=123
123 % 10 = 3
So 1229012-68-3 is a valid CAS Registry Number.

1229012-68-3SDS

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 2,9-dichloro-4,7-diphenyl-1,10-phenanthroline

1.2 Other means of identification

Product number -
Other names -

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:1229012-68-3 SDS

1229012-68-3Relevant academic research and scientific papers

BIS-PHENANTHROLINE IRON MACROCYCLE COMPLEX FOR OXYGEN REDUCTION REACTION

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Page/Page column 50; 52, (2020/09/27)

Disclosed are compounds, compositions, and methods useful for the oxygen reduction reaction (ORR) and capable of operating efficiently at low overpotentials.

ELECTRONIC DEVICE INCLUDING PHENANTHROLINE DERIVATIVE

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Page/Page column 13, (2012/03/27)

There is provided an organic electronic device having an anode, a hole injection layer, a photoactive layer, an electron transport layer, and a cathode. At least one of the photoactive layer and the electron transport layer includes a compound having Formula I where: R1 is the same or different and can be phenyl, biphenyl, naphthyl, naphthylphenyl, triphenylamino, or carbazolylphenyl;and one of the following conditions is met:(i) R2=R3 and is H, phenyl, biphenyl, naphthyl, naphthylphenyl, arylanthracenyl, phenanthryl, triphenylamino, or carbazolylphenyl; or(ii) R2 is H or phenyl; and R3 is phenyl, biphenyl, naphthyl, naphthylphenyl, arylanthracenyl, phenanthryl, triphenylamino, and carbazolylphenyl; When both R1 are phenyl, R2 and R3 can be 2-naphthyl, naphthylphenyl, arylanthracenyl, 9-phenanthryl, triphenylamino, or m-carbazolylphenyl.

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