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66433-95-2

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66433-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66433-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,3 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66433-95:
(7*6)+(6*6)+(5*4)+(4*3)+(3*3)+(2*9)+(1*5)=142
142 % 10 = 2
So 66433-95-2 is a valid CAS Registry Number.

66433-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[6-[(2-formylphenoxy)methyl]pyridin-2-yl]methoxy]benzaldehyde

1.2 Other means of identification

Product number -
Other names 2,6-Bis-(2-formyl-phenoxymethyl)-pyridine

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:66433-95-2 SDS

66433-95-2Relevant articles and documents

The syntheses of nitrogen-oxygen donor macrocycles containing pyridine ring

Zhao,Feng Qin Wang,Lai Jin Tian

, p. 781 - 783 (2001)

Five new nitrogen-oxygen mixed donor macrocycles have been prepared by condensation of 2,6-bis [(2-formylphenyl)oxymethyl]pyridine with different diamino compounds in hot methanol, followed by a one-pot reduction of the intermediate bis-Schiff base. All the macrocycles were identified by elemental analysis, and ir, uv, and nmr spectroscopy.

Microwave assisted multi-component synthesis of novel bis(1,4-dihydropyridines) based arenes or heteroarenes

Sanad, Sherif M. H.,Kassab, Refaie M.,Abdelhamid, Ismail A.,Elwahy, Ahmed H. M.

, p. 910 - 924 (2016/07/06)

A synthesis of novel bis-1,4-DHPs was reported. Two possible synthetic approaches for these compounds were investigated. In the first approach the monopodal 1,4-DHPs were used as building blocks for the construction of the target molecules via a simple al

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.

experimental part, 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

Sulfur-containing mixed-donor tribenzo-macrocycles and their endo-and exocyclic supramolecular silver(I) and copper(I) complexes

Kang, Eun-Ju,Lee, So Young,Lee, Hayan,Lee, Shim Sung

scheme or table, p. 7510 - 7520 (2010/09/17)

New sulfur-containing mixed-donor macrocycles L1-L4 with different donor sets and/or ring sizes (L1, 20-membered O 3S2; L2, 20-membered NO2S 2; L3, 20-membe

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