2-​Propenoic acid, 3-​methoxy-

95%

Reagent Code: #223324
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CAS Number 6162-52-3

science Other reagents with same CAS 6162-52-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 102.0886 g/mol
Formula C₄H₆O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reactive monomer in the synthesis of specialty polymers and copolymers, this compound contributes to the production of adhesives, coatings, and sealants with enhanced flexibility and adhesion properties. Its methoxy group imparts polarity and influences solubility, making it suitable for formulations requiring improved compatibility with polar solvents. It is also employed in controlled radical polymerization techniques to design functional polymers for advanced materials, including drug delivery systems and surface modifiers. Additionally, it finds use in the development of photoresists and electronic materials due to its ability to participate in UV-curable resin systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,000.00
inventory 250mg
10-20 days ฿28,800.00
inventory 1g
10-20 days ฿64,000.00

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2-​Propenoic acid, 3-​methoxy-
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Used primarily as a reactive monomer in the synthesis of specialty polymers and copolymers, this compound contributes to the production of adhesives, coatings, and sealants with enhanced flexibility and adhesion properties. Its methoxy group imparts polarity and influences solubility, making it suitable for formulations requiring improved compatibility with polar solvents. It is also employed in controlled radical polymerization techniques to design functional polymers for advanced materials, including d

Used primarily as a reactive monomer in the synthesis of specialty polymers and copolymers, this compound contributes to the production of adhesives, coatings, and sealants with enhanced flexibility and adhesion properties. Its methoxy group imparts polarity and influences solubility, making it suitable for formulations requiring improved compatibility with polar solvents. It is also employed in controlled radical polymerization techniques to design functional polymers for advanced materials, including drug delivery systems and surface modifiers. Additionally, it finds use in the development of photoresists and electronic materials due to its ability to participate in UV-curable resin systems.

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