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19243-95-9

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19243-95-9 Usage

Description

N-(4-HYDROXYPHENYL)METHACRYLAMIDE is an organic compound with the molecular formula C10H11NO2. It is a monomer that possesses a hydroxyphenyl group and a methacrylamide group, which allows it to be polymerized and used in various applications.

Uses

Used in Biomedical Applications:
N-(4-HYDROXYPHENYL)METHACRYLAMIDE is used as a monomer for creating polymer substrates that support cell expansion and differentiation. Its hydroxyphenyl and methacrylamide groups enable interactions with biological molecules, making it a promising candidate for applications in tissue engineering and regenerative medicine.
Used in Lithographic Applications:
In the field of lithography, N-(4-HYDROXYPHENYL)METHACRYLAMIDE is used as a monomer to produce polymers that can be employed as resists or other components in the lithographic process. Its properties allow for precise patterning and etching of materials, which is crucial for the fabrication of microelectronic devices and other microscale structures.
Used in Polymer Synthesis:
N-(4-HYDROXYPHENYL)METHACRYLAMIDE is used as a monomer in the synthesis of various polymers. The resulting polymers can have unique properties, such as enhanced biocompatibility or improved mechanical strength, making them suitable for a wide range of applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 19243-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,4 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19243-95:
(7*1)+(6*9)+(5*2)+(4*4)+(3*3)+(2*9)+(1*5)=119
119 % 10 = 9
So 19243-95-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO2/c1-7(2)10(13)11-8-3-5-9(12)6-4-8/h3-6,12H,1H2,2H3,(H,11,13)

19243-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-hydroxyphenyl)-2-methylprop-2-enamide

1.2 Other means of identification

Product number -
Other names ACRYLANILIDE,4'-HYDROXY-2-METHYL

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:19243-95-9 SDS

19243-95-9Relevant articles and documents

Nitric Oxide (NO) Endows Arylamine-Containing Block Copolymers with Unique Photoresponsive and Switchable LCST Properties

Hu, Jinming,Whittaker, Michael R.,Quinn, John F.,Davis, Thomas P.

, p. 2741 - 2749 (2016/05/10)

The fabrication of materials that are responsive to endogenous gasotransmitter molecules (i.e., nitric oxide, hydrogen sulfide, and carbon monoxide) has emerged as an area of increasing research interest. In the case of nitric oxide (NO), o-phenylenediami

Two-layer imageable element comprising thermally reversible polymers

-

, (2008/06/13)

The present invention includes a two-layer imageable element, including: a substrate, a top layer including a first thermally imageable composition including (a) a first thermally sensitive supramolecular polymer or (b) a thermally imageable composition free of the first thermally sensitive supramolecular polymer; and disposed between the substrate and the top layer, a bottom layer including a second thermally imageable composition, which includes a second thermally sensitive supramolecular polymer. The present invention also includes a method of producing the imaged element.

Sunblocking polymers and their formulation

-

, (2008/06/13)

Novel polymeric compositions and their intermediates are provided, providing for broad range protection from ultraviolet radiation. Acryl polymers comprising at least two different ultraviolet absorbing moieties having different light absorbing ranges are employed in conjunction with another hydrophilic monomer to provide sunscreen formulations for invisibility, and enhanced protection, without deleterious effects in the dermis.

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