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Benzenamine, 2,2'-[2,6-pyridinediylbis(methyleneoxy)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109176-72-9

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109176-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109176-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,1,7 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109176-72:
(8*1)+(7*0)+(6*9)+(5*1)+(4*7)+(3*6)+(2*7)+(1*2)=129
129 % 10 = 9
So 109176-72-9 is a valid CAS Registry Number.

109176-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[6-[(2-aminophenoxy)methyl]pyridin-2-yl]methoxy]aniline

1.2 Other means of identification

Product number -
Other names AmbscL33/078

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:109176-72-9 SDS

109176-72-9Downstream Products

109176-72-9Relevant academic research and scientific papers

Synthesis, structural characterization and metal inclusion properties of 18-, 20- and 22-membered oxaazacyclophanes and oxaazacalix[4]arene analogues: Macrocyclic amine and schiff base receptors with variable NxO y donor sets

Moreno-Corral, Ramon,Hoepfl, Herbert,MacHi-Lara, Lorena,Lara, Karen O.

, p. 2148 - 2162 (2011/05/09)

A series of oxaazacyclophanes and oxaazacalix[4]arene analogues with 18-, 20- and 22-membered rings have been synthesized from diamine and dialdehyde building blocks and structurally characterized by spectroscopic methods. One diamine precursor and four macrocycles have additionally been analysed by single-crystal X-ray diffraction. Two of the oxaazacalix[4]arene analogues were employed for metal ion complexation studies based on UV/Vis absorption spectroscopy, showing both compounds to be able to form complexes with Cu 2+ and Zn2+. Copyright

The synthesis, X-ray structure and metal cation complexation properties of colored crown with two heterocyclic residues as a part of macrocycle

Wagner-Wysiecka,Luboch,Fonari

, p. 1319 - 1330 (2008/12/21)

New azocrown ether with pyrrole and pyridine as parts of macrocycle was synthesized. Metal cation complexation was investigated in acetonitrile and in acetonitrile-water mixture with the use of UV/VIS spectroscopy. Structure of the macrocycle was studied

Studies of Metal-ion Recognition. The Interaction of CoII, NiII, and CuII with New Oxygen-Nitrogen Donor Macrocycles; X-Ray Structures of Complexes of CuII and NiII with a 15-Membered O2N3 Derivative

Fenton, David E.,Murphy, Brian P.,Leong, Anthony J.,Lindoy, Leonard F.,Bashall, Alan,McPartlin, Mary

, p. 2543 - 2554 (2007/10/02)

Tetrahydroborate reduction of a range of Schiff-base di-imine macrocycles, prepared by template cyclization reactions on manganese(II) or lead(II), has afforded a series of structurally related metal-free macrocycles incorporating both oxygen and nitrogen

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