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Benzenamine, 4,4'-[[2,2-bis[(4-aminophenoxy)methyl]-1,3-propanediyl]bis(oxy)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60713-81-7

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60713-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60713-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,1 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60713-81:
(7*6)+(6*0)+(5*7)+(4*1)+(3*3)+(2*8)+(1*1)=107
107 % 10 = 7
So 60713-81-7 is a valid CAS Registry Number.

60713-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tetrakis[(4-aminophenoxy)methyl]methane

1.2 Other means of identification

Product number -
Other names Tetra-O-(4-amino-phenyl)-pentaerythrit

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:60713-81-7 SDS

60713-81-7Relevant academic research and scientific papers

Novel compound tetra[(p-aminophenoxy)methyl]methane and synthesis method thereof

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Paragraph 0041; 0046; 0051, (2017/08/25)

The present invention discloses a compound tetra[(p-aminophenoxy)methyl]methane, which has the following molecular structure formula defined in the specification. The synthesis method mainly comprises two steps that 1, pentaerythrityl tetrabromide and p-acetamidophenol are subjected to a Williamson synthesis reaction to obtain tetra[(p-acetamidophenoxy)methyl]methane; and 2, the tetra[(p-acetamidophenoxy)methyl]methane is subjected to a hydrolysis reaction to obtain the tetra[(p-aminophenoxy)methyl]methane. According to the present invention, the compound contains four amine groups and the stable benzene ring structure, and the amine group and the benzene ring are directly connected and can be used in the curing of the epoxy resin system so as to rapidly cure the epoxy resin and make the cured product have good heat resistance and good mechanical property.

Molecular Tectonics. Porous Hydrogen-Bonded Networks Built from Derivatives of Pentaerythrityl Tetraphenyl Ether

Laliberte, Dominic,Maris, Thierry,Wuest, James D.

, p. 1776 - 1787 (2007/10/03)

The symmetric four-armed geometry of pentaerythrityl tetraphenyl ether (5) makes it a valuable starting point for building complex molecular and supramolecular structures. In particular, it provides a core to which multiple sites of attractive intermolecular interaction can be attached, thereby creating compounds predisposed to form complex networks by association. To facilitate exploitation of the pentaerythrityl tetraphenyl ether core in such ways, we have prepared more than 20 new derivatives by efficient methods. Of special interest are compounds 3 and 4, which incorporate four diaminotriazine groups attached to the meta and para positions of the pentaerythrityl tetraphenyl ether core. Crystallization of compounds 3 and 4 from DMSO/dioxane is directed by hydrogen bonding of the diaminotriazine groups according to well-established motifs, thereby producing three-dimensional networks. In forming these networks, each molecule of compound 3 forms a total of 12 hydrogen bonds with six others, whereas each molecule of compound 4 forms a total of 16 hydrogen bonds with four others. Both networks are highly porous and define significant interconnected channels for the inclusion of guests. In crystals of compounds 3 and 4, the fraction of the volume accessible to guests is 66% and 57%, respectively. In both cases, the pentaerythrityl tetraphenyl ether cores adopt conformations that deviate substantially from tetrahedral geometry. It is noteworthy that the inherent flexibility of the core does not favor the formation of close-packed guest-free structures.

Alkylated urea and triaminotriazine compounds and phase change inks containing same

-

, (2008/06/13)

Disclosed are compounds of the formulae wherein Z is a group of the formula —OR1, a group of the formula —SR1, or a group of the formula —NR1R2, Y is a group of the formula —OR3, a group of the formul

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