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24812-82-6

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24812-82-6 Usage

Description

2,2'-(3-NITROPHENYLIMINO)-DIETHANOL, also known as N,N'-Bis(3-nitrophenyl)ethylenediamine, is a chemical compound with the molecular formula C12H12N2O4. It is a chelating agent and a ligand for metal ions, commonly utilized in coordination chemistry and metal-based catalysts. This chemical is used in various industrial applications, including in the production of polymers, dyes, and pharmaceuticals. It has also demonstrated potential antimicrobial properties, making it of interest for use in the development of antimicrobial agents. Additionally, its chelating properties make it useful in analytical chemistry for the detection and determination of metal ions in complex samples.

Uses

Used in Chemical Industry:
2,2'-(3-NITROPHENYLIMINO)-DIETHANOL is used as a chelating agent and ligand for metal ions in coordination chemistry and metal-based catalysts for various chemical reactions.
Used in Polymer Production:
2,2'-(3-NITROPHENYLIMINO)-DIETHANOL is used as a component in the production of polymers to enhance their properties and performance.
Used in Dye Industry:
2,2'-(3-NITROPHENYLIMINO)-DIETHANOL is used as a component in the production of dyes to improve their color and stability.
Used in Pharmaceutical Industry:
2,2'-(3-NITROPHENYLIMINO)-DIETHANOL is used as a component in the development of pharmaceuticals due to its potential antimicrobial properties.
Used in Analytical Chemistry:
2,2'-(3-NITROPHENYLIMINO)-DIETHANOL is used as a chelating agent for the detection and determination of metal ions in complex samples.

Check Digit Verification of cas no

The CAS Registry Mumber 24812-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24812-82:
(7*2)+(6*4)+(5*8)+(4*1)+(3*2)+(2*8)+(1*2)=106
106 % 10 = 6
So 24812-82-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O4/c13-6-4-11(5-7-14)9-2-1-3-10(8-9)12(15)16/h1-3,8,13-14H,4-7H2

24812-82-6SDS

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-[N-(2-hydroxyethyl)-3-nitroanilino]ethanol

1.2 Other means of identification

Product number -
Other names N,N-di-(2-Hydroxyethyl)-m-nitroaniline

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:24812-82-6 SDS

24812-82-6Relevant articles and documents

Pyrazolo [1, 5 - a] pyrimidine nitrogen mustard derivative and its preparation method and tumor therapeutic use

-

Paragraph 0115; 0116; 0117; 0118; 0119, (2017/08/02)

The invention relates to pyrazolo[1,5-alpha] pyrimidine nitrogen mustard derivatives or medical salts thereof, as well as application of the pyrazolo[1,5-alpha] pyrimidine nitrogen mustard derivatives or the medical salts thereof. The pyrazolo[1,5-alpha] pyrimidine nitrogen mustard derivatives and the medical salts thereof have the structure shown as the formula I. Pharmacological experiments show that the pyrazolo[1,5-alpha] pyrimidine nitrogen mustard derivatives and the medical salts thereof have inhibiting effects on the proliferation of various tumor cells. Moreover, the pyrazolo[1,5-alpha] pyrimidine nitrogen mustard derivatives are small in toxicity, have the advantages of selectivity on tumor cells, and are dual-functional anti-tumor drugs. Meanwhile, the pyrazolo[1,5-alpha] pyrimidine nitrogen mustard derivatives are easy to synthesize, and the overall yields are high. All the advantages show that the pyrazolo[1,5-alpha] pyrimidine nitrogen mustard derivatives have great potential of being anti-tumor drugs.

Synthesis, crystal structure and biological activity of novel diester cyclophanes

Zhang, Pengfei,Yang, Bingqin,Fang, Xianwen,Cheng, Zhao,Yang, Meipan

, p. 1771 - 1775 (2013/03/13)

A series of novel diester cyclophanes was synthesized by esterification of 1,2-benzenedicarbonyl chloride with eight different diols under high dilution conditions. The structures of the compounds were verified by elemental analysis, 1H nuclear magnetic resonance (NMR), IR spectroscopy and high resolution mass spectrometry (HRMS). The crystal structures of two compounds were characterized by single crystal X-ray diffractometry (XRD). All the new cyclophanes were evaluated for biological activities and the results showed that some of these compounds have low antibacterial or antifungal activities.

Lewis acids catalyzed ring-opening reactions of methylenecyclopropanes and epoxides in supercritical carbon dioxide or modified supercritical carbon dioxide with perfluorocarbon

Shi, Min,Chen, Yu

, p. 219 - 227 (2007/10/03)

The reactions of methylenecyclopropanes (MCPs) and epoxides with alcohols and aromatic amines can be carried out in supercritical carbon dioxide (scCO2) or modified scCO2 with perfluorocarbon which offer a way to synthesize various alcohols, amino-alcohols, homoallylic ethers, and amines under an environmentally benign condition.

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