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89579-23-7

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89579-23-7 Usage

Melting Point

110-112°C
The temperature range at which the compound transitions from a solid to a liquid state.

Boiling Point

431.8°C
The temperature at which the compound changes from a liquid to a gaseous state.

Solubility

Insoluble in water, soluble in organic solvents
Does not dissolve in water but dissolves easily in certain organic solvents.

Usage

Crosslinking agent in resins and polymers
Enhances the strength and stability of resins and polymers by forming a three-dimensional network structure.

Applications

Manufacturing of adhesives, coatings, and plastics
Widely used in various industries to produce strong and durable materials.

Fragrance Ingredient

In perfumes and cosmetics

Safety Precautions

Harmful if ingested or upon contact with skin or eyes
Requires proper handling and protective measures to avoid potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 89579-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,7 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89579-23:
(7*8)+(6*9)+(5*5)+(4*7)+(3*9)+(2*2)+(1*3)=197
197 % 10 = 7
So 89579-23-7 is a valid CAS Registry Number.

89579-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Phenylenebis(methylenoxy-2-benzaldehyde)

1.2 Other means of identification

Product number -
Other names O,O'-diethyl-triethylene glycol

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:89579-23-7 SDS

89579-23-7Relevant articles and documents

A comparative molecular structure – NLO activity study of ortho-bridged dibenzaldehydes: Synthesis, crystal structure, SHG, and DFT studies

Jothi, A. Irudaya,Paul, M. Wilson Bosco,Alexander

, (2021/11/16)

Structural and second order nonlinear optical characteristics of four ortho-bridged dibenzaldehydes with alkyloxy- and xylenyloxy linkers are compared from the XRD, UV-Vis-NIR spectroscopic, SHG, and DFT studies. Interruption of electron polarization by π

Molecular-strain engineering of double-walled tetrahedra

Bian, Lifang,Jiang, Liang,Liang, Yimin,Liu, Jiali,Liu, Zhichang,Lu, Xingyu,Miao, Xiaohe,Tang, Min,Wang, Shangshang,Wu, Lin

supporting information, p. 2160 - 2174 (2021/08/13)

The synthesis of multi-walled nanostructures represents a formidable challenge owing to the limitations imposed by existing synthetic strategies. Herein, we report a strategy involving molecular-strain engineering (MSE) for constructing double-walled polyhedra from strained bow-shaped macrocycles called molecular bows (MBs). As a proof of concept, four double-walled tetrahedra have been assembled from L-shaped dual-panels subtending ~70.5° and producing MBs, which incorporate porphyrin and o-xylylene units, forming strained shape-persistent conformations. The head-to-tail closed-loop stacking of these units, driven by complementary non-covalent bonding interactions, leads to a large porphyrin-lined tetrahedron encapsulating a small o-xylylene-lined tetrahedron. The synergistic aromatic shielding effects emanating from the porphyrin tetrahedron result in the largest upfield chemical shifts of ?7.7 ppm for protons and ?8.8 ppm for carbons from those for the free dual panels. This demonstration, which features the launching of MSE for constructing sophisticated supramolecular nanostructures, could herald a fresh approach to the fabrication of multi-porphyrin photocatalytic systems.

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

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