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bis[4-((3-pyridylmethylidene)amino)phenyl]methane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

304481-20-7

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304481-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 304481-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,4,8 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 304481-20:
(8*3)+(7*0)+(6*4)+(5*4)+(4*8)+(3*1)+(2*2)+(1*0)=107
107 % 10 = 7
So 304481-20-7 is a valid CAS Registry Number.

304481-20-7Relevant academic research and scientific papers

Cage-to-Cage Cascade Transformations

Bandi, Sreenivasulu,Chand, Dillip Kumar

, p. 10330 - 10335 (2016/07/21)

A series of Pd2L4-type binuclear self-assembled coordination cages (1–4), where L stands for a nonchelating bidentate ligand, were prepared. The strategies adopted for the synthesis of the cages were: combination of PdIIwith 1) a selected ligand or 2) subcomponents of the ligand. Highly efficient cage-to-cage transformation reactions are demonstrated by suitable covalent modification (from 1 to 2 or 3 or 4) or ligand-exchange reactions (from 1 to 2 or 3 or 4; from 2 to 3 or 4). Thus, new cascade transformations (from 1 to 2 to 3; from 1 to 2 to 4) are achieved beautifully.

Synthesis of novel paracyclophanes with linear P,N-containing spacers

Ignat'eva,Balueva,Karasik,Kulikov,Kozlov,Latypov,Loennecke,Hey-Hawkins,Sinyashin

, p. 1828 - 1837 (2008/09/20)

Condensation of bis(hydroxymethyl)mesityl-and bis(hydroxymethyl) phenylphosphines with N,N′-disubstituted bis(4-aminophenyl)methanes and bis(4-amino-3-carboxyphenyl)methane occurred as covalent self-assembly spontaneously giving a mixture of trans-and cis-diastereomers of 1,5,19,23-tetra-R′-3,21-di-R-1,5,19,23-tetraaza-3,21-diphospha[5.1.5.1] paracyclophanes as the major products. The trans-isomer (R is mesityl; R′ is methyl) was isolated in the individual state and structurally characterized by X-ray diffraction analysis. Sulfurization of macrocyclic diphosphines (R = Ph; R′ is 3-pyridylmethyl or 4-pyridylmethyl) gave the corresponding diphosphine disulfides, the trans-stereoisomer being isolated in the individual state.

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