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3-(4-(hydroxymethyl)phenoxy)phthalonitrile is a chemical compound characterized by the molecular formula C15H9NO4. It is a derivative of phthalonitrile, which is known for its unique chemical structure and properties. This versatile compound is primarily used in the production of dyes and pigments, as well as in the synthesis of organic materials. Its potential applications extend to various industrial processes, including the manufacturing of polymers and coatings.

649553-08-2

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649553-08-2 Usage

Uses

Used in Dye and Pigment Production:
3-(4-(hydroxymethyl)phenoxy)phthalonitrile is used as a key intermediate in the production of dyes and pigments. Its unique chemical structure contributes to the color and stability of these products, making it an essential component in this application.
Used in Organic Material Synthesis:
3-(4-(hydroxymethyl)phenoxy)phthalonitrile is utilized in the synthesis of various organic materials due to its reactive functional groups and compatibility with other chemical entities. Its involvement in organic synthesis allows for the creation of new materials with specific properties tailored for different applications.
Used in Polymer Manufacturing:
3-(4-(hydroxymethyl)phenoxy)phthalonitrile is used as a monomer or a building block in the manufacturing of polymers. Its incorporation into polymer structures can enhance properties such as color, stability, and durability, making it a valuable component in the polymer industry.
Used in Coating Industry:
In the coating industry, 3-(4-(hydroxymethyl)phenoxy)phthalonitrile is used to improve the performance of coatings. Its addition can enhance the color, durability, and resistance to environmental factors, resulting in coatings with superior protective qualities.
Overall, 3-(4-(hydroxymethyl)phenoxy)phthalonitrile is a multifaceted chemical compound with a broad spectrum of applications across various industries, primarily due to its unique chemical structure and properties. Its versatility makes it a valuable asset in the development of new materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 649553-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,9,5,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 649553-08:
(8*6)+(7*4)+(6*9)+(5*5)+(4*5)+(3*3)+(2*0)+(1*8)=192
192 % 10 = 2
So 649553-08-2 is a valid CAS Registry Number.

649553-08-2SDS

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 3-(4-(Hydroxymethyl)phenoxy)phthalonitrile

1.2 Other means of identification

Product number -
Other names 3-[4-(hydroxymethyl)phenoxy]benzene-1,2-dicarbonitrile

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:649553-08-2 SDS

649553-08-2Relevant academic research and scientific papers

Synthesis of tetrasubstituted Zn(II)-phthalocyanines carrying four carboranyl-units as potential BNCT and PDT agents

Giuntini, Francesca,Raoul, Yann,Dei, Donata,Municchi, Moira,Chiti, Giacomo,Fabris, Clara,Colautti, Paolo,Jori, Giulio,Roncucci, Gabrio

, p. 2979 - 2982 (2007/10/03)

The synthesis of two tetrasubstituted zinc(II)phthalocyanines carrying four carbon-carbon linked o-carboranyl-units (40 boron atoms, 27.5% boron by weight) is presented. In an in vitro model test the new compounds showed a good photosensitizing efficiency

Synthesis and antimycotic activity of new unsymmetrical substituted zinc phthalocyanines

Cosimelli, Barbara,Roncucci, Gabrio,Dei, Donata,Fantetti, Lia,Ferroni, Fiammetta,Ricci, Micaela,Spinelli, Domenico

, p. 10025 - 10030 (2007/10/03)

The synthesis of new unsymmetrical substituted zinc phthalocyanines derivatives has been described; moreover the photodynamic activity of some compounds tested against Candida albicans has been reported.

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