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N-hydroxy-2-(pyridin-2-yl)-N-[2-(pyridin-2-yl)ethyl]ethanamine is a complex organic compound with the molecular formula C15H18N3O. It is characterized by the presence of a hydroxyl group (-OH), two pyridine rings, and an ethylamine chain. This molecule is known for its potential applications in pharmaceutical research, particularly as a precursor in the synthesis of various biologically active compounds. Its structure features a central ethanamine (ethylamine) backbone with a hydroxyl group attached to the nitrogen atom, and two pyridine rings, one directly linked to the nitrogen and the other to the ethyl chain. The compound's unique structure and properties make it a subject of interest in the development of new drugs and chemical entities.

6965-67-9

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6965-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6965-67-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6965-67:
(6*6)+(5*9)+(4*6)+(3*5)+(2*6)+(1*7)=139
139 % 10 = 9
So 6965-67-9 is a valid CAS Registry Number.

6965-67-9SDS

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 N,N-bis(2-pyridin-2-ylethyl)hydroxylamine

1.2 Other means of identification

Product number -
Other names Pyridine, 2,2‘-[(hydroxyimino)diethylene]di-

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:6965-67-9 SDS

6965-67-9Upstream product

6965-67-9Relevant academic research and scientific papers

Effect of Chelate Ring Size of Binuclear Copper(II) Complexes on Catecholase Activity and DNA Cleavage

Homrich, Alana M.,Farias, Giliandro,Amorim, Suélen M.,Xavier, Fernando R.,Gariani, Rogério A.,Neves, Ademir,Terenzi, Hernán,Peralta, Rosely A.

, p. 1710 - 1721 (2021)

Catecholase activity of dicopper(II) complexes containing different numbers of chelate members in the pyridine groups of the ligand was studied to identify a functional model for copper enzyme catechol oxidase. Complexes [CuII(μ-OH)CuII/s

A new synthesis of bis(2-{pyrid-2-yl}ethyl)amine (LH) from bis(2-{pyrid-2-yl}ethyl)hydroxylamine (LOH), and the copper-dependent reduction of LOH to LH

Leaver, Stewart A.,Palaniandavar, Mallayan,Kilner, Colin A.,Halcrow, Malcolm A.

, p. 4224 - 4225 (2003)

Solutions of [CuCl2LOH], and other reaction mixtures containing LOH and Cu(II) or Cu(I) salts, degrade to yield dark green or brown residues containing the LH ligand. In contrast, [MCl2LOH] (M = Zn, Ni, Co) are indefinitely stable in solution and the solid state.

Unprecedented synthesis of symmetrical azines from alcohols and hydrazine hydrate using nickel based NNN-pincer catalyst: An experimental and computational study

Shiekh, Bilal Ahmad,Kaur, Damanjit,Godara, Sachin Kumar

, p. 19 - 23 (2019/03/02)

Azines are having widespread applications in both industry as well as synthetic chemistry. Thus new catalytic synthetic protocols are desirable as they are greener alternatives than traditional methods of synthesis. Thus, herein a novel earth abundant nickel based NNN-pincer catalyst Ni(BPEA)(Cl2) is synthesized for the first time for the direct transformation of alcohols and hydrazine hydrate into symmetrical azines. This catalytic reaction is accompanied by dehydrogenative coupling of alcohols and hydrazine hydrate and is carried out in presence of a base. Theoretical calculations supported by experimental evidence have been performed for understanding the mechanistic insights of the reaction.

METHOD OF PRODUCING PHENOLIC COMPOUND

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Page/Page column 11; 13, (2017/04/27)

PROBLEM TO BE SOLVED: To provide a method of efficiently producing a phenolic compound by direct oxidation of an aromatic compound. SOLUTION: A phenolic compound is produced by oxidation of an aromatic compound by an oxidant in the presence of a binuclear nickel complex having a ligand being a compound represented by the formula (I) or (II) in the figure. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Exploiting 1,2,3-Triazolium Ionic Liquids for Synthesis of Tryptanthrin and Chemoselective Extraction of Copper(II) Ions and Histidine-Containing Peptides

Li, Hsin-Yi,Chen, Chien-Yuan,Cheng, Hui-Ting,Chu, Yen-Ho

, (2016/11/02)

Based on a common structural core of 4,5,6,7-Tetrahydro[1,2,3]triazolo[1,5-A]pyridine, a number of bicyclic triazolium ionic liquids 1-3 were designed and successfully prepared. In our hands, this optimized synthesis of ionic liquids 1 and 2 requires no chromatographic separation. Also in this work, ionic liquids 1, 2 were shown to be efficient ionic solvents for fast synthesis of tryptanthrin natural product. Furthermore, a new affinity ionic liquid 3 was tailor-synthesized and displayed its effectiveness in chemoselective extraction of both Cu(II) ions and, for the first time, histidine-containing peptides.

Modification and optimization of the bis-picolylamide-based relay protection for carboxylic acids to be cleaved by unusual complexation with Cu2+ salts

Mundinger, Stephan,Jakob, Uwe,Bichovski, Plamen,Bannwarth, Willi

, p. 8968 - 8979,12 (2012/12/11)

A simple modification of our recently published protection scheme for carboxylic acids as amides resulted in a new protecting group with significantly improved properties. It requires shorter reaction times for deprotection and allows us to replace Cu(OTf)2 by CuCl2, indicating at the same time the importance of the nature of the anion of the Cu2+ source. Since the new scheme fulfills all criteria required for an ideal protection group it should find widespread application in synthetic organic chemistry.

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