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4-{[2-(acryloyloxy)ethoxy]carbonyl}benzene-1,3-dicarboxylic acid is a complex organic compound with the molecular formula C15H14O8. It is characterized by a benzene ring with two carboxyl groups at the 1 and 3 positions, and a unique functional group at the 4 position. This functional group consists of a carbonyl group attached to an ethoxy chain, which in turn is connected to an acryloyloxy group. The acryloyloxy group is significant as it contains a vinyl double bond, making it reactive for polymerization processes. 4-{[2-(acryloyloxy)ethoxy]carbonyl}benzene-1,3-dicarboxylic acid is potentially used in the synthesis of polymers and other advanced materials due to its ability to participate in cross-linking reactions. Its structure provides a bridge between aromatic and aliphatic moieties, which can influence the properties of the resulting polymers, such as their thermal stability, mechanical strength, and chemical resistance.

84732-27-4

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84732-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84732-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,3 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84732-27:
(7*8)+(6*4)+(5*7)+(4*3)+(3*2)+(2*2)+(1*7)=144
144 % 10 = 4
So 84732-27-4 is a valid CAS Registry Number.

84732-27-4SDS

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 4-(2-prop-2-enoyloxyethoxycarbonyl)benzene-1,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names -

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

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More Details:84732-27-4 SDS

84732-27-4Downstream Products

84732-27-4Relevant academic research and scientific papers

UV-assisted direct ink write printing of fully aromatic Poly(amide imide)s: Elucidating the influence of an acrylic scaffold

Arrington, Clay B.,Long, Timothy E.,Rau, Daniel A.,Williams, Christopher B.

, (2021)

High performance engineering thermoplastics exhibit excellent thermomechanical performance and chemical resistance, however, the rigid polymeric main chains that are derived from highly or fully aromatic repeating units impose processing challenges. The design of photo-reactive precursors now enables additive manufacturing of poly(amide imide) (PAI) precursor organo-gels via UV-assisted direct ink write (DIW) printing. Solution rheology revealed prerequisite high solution viscosities and shear thinning behavior of organic solutions of the PAI precursors. Additionally, photorheology of PAI precursors exhibited rapid gelation and high gel strengths, enabling production of self-supporting organo-gels that are necessary for successful DIW. Thermal post-treatment of the printed organo-gels revealed isotropic linear shrinkage as low as 26% during drying and imidization. The reduced chain rigidity of the poly(amide imide), relative to fully-aromatic polyimides, prevented quantitative thermal removal of the poly (hydroxyethyl acrylate) (poly(HEA)) scaffold, resulting in a decreased glass transition temperature (263 °C) relative to commercial PAI (290 °C). Moreover, crosslinking of the PHEA during thermal imidization limited scaffold removal upon solvent extraction, however, suggested the formation of novel multiphase polymers. Selective dissolution of the PAI from the crosslinked PHEA enabled assessment of the role of the scaffold on thermomechanical properties and characterization of printed PAI. Spectroscopic and thermal analysis confirmed the formation of the desired PAI composition with this photochemical synthetic method.

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