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9-Fluorenyl methacrylate is a unique monomer characterized by the presence of a fluorenyl group, which imparts fluorescent properties, and a methacrylate part, ensuring its incorporation into polymers due to its structural similarity to the methyl methacrylate monomer. It is synthesized from 9-hydroxyfluoren alcohol, which is coupled with methacrylate anhydride.

46969-53-3

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46969-53-3 Usage

Uses

Used in Polymer Industry:
9-Fluorenyl methacrylate is used as a monomer for the development of polymers with enhanced fluorescent properties. The incorporation of this monomer into polymers allows for the creation of materials with potential applications in various fields, such as sensors, imaging, and optical devices.
Used in Fluorescent Materials:
9-Fluorenyl methacrylate is used as a key component in the production of fluorescent materials. Its ability to fluoresce makes it a valuable addition to the development of materials that can be used in the creation of light-emitting diodes (LEDs), organic light-emitting diodes (OLEDs), and other light-emitting applications.
Used in Research and Development:
9-Fluorenyl methacrylate is utilized as a research tool for studying the properties and behavior of polymers containing fluorescent moieties. Its unique combination of fluorescence and polymer compatibility makes it an essential material for advancing the understanding of polymer science and the development of new materials with specific properties and applications.
Used in Biomedical Applications:
9-Fluorenyl methacrylate can be used as a component in the development of biocompatible materials for medical applications. Its fluorescent properties can be harnessed for imaging and diagnostic purposes, while its polymer compatibility allows for the creation of materials that can be tailored to specific medical needs.
Used in Environmental Monitoring:
9-Fluorenyl methacrylate can be employed in the development of environmental sensors that utilize fluorescence as a means of detecting and monitoring pollutants or other environmental factors. The incorporation of this monomer into sensor materials can lead to the creation of more sensitive and selective detection systems.

Check Digit Verification of cas no

The CAS Registry Mumber 46969-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,9,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 46969-53:
(7*4)+(6*6)+(5*9)+(4*6)+(3*9)+(2*5)+(1*3)=173
173 % 10 = 3
So 46969-53-3 is a valid CAS Registry Number.

46969-53-3 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Aldrich

  • (733342)  9-Fluorenylmethacrylate  97%

  • 46969-53-3

  • 733342-1G

  • 538.20CNY

  • Detail
  • Aldrich

  • (733342)  9-Fluorenylmethacrylate  97%

  • 46969-53-3

  • 733342-5G

  • 1,831.05CNY

  • Detail

46969-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 9H-fluoren-9-yl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 9-FMA

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:46969-53-3 SDS

46969-53-3Downstream Products

46969-53-3Relevant academic research and scientific papers

Synthesis and self-assembly of polyhydroxylated and electropolymerizable block copolymers

Barik, Satyananda,Valiyaveettil, Suresh

, p. 2217 - 2227 (2014)

A facile synthetic strategy for preparing hydroxylated polymethacrylate amphiphilic block copolymers (PCzMMA-b-PBMMA, PFlMMA-b-PBMMA) incorporated with primary and secondary hydroxyl groups and electroactive moieties along the polymer backbone is reported

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