82200-53-1

Basic information

• Product Name: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester
• Synonyms: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester;4-Methoxyphenyl-4-(6-(acryloyloxy)hexyloxy)benzoate;4-[[6-[(1-Oxo-2-propenyl)oxy]hexyl]oxy]benzoic acid 4-Methoxyphenyl ester;Benzoic acid,4-[[6-[(1-oxo-2-propen-1-yl)oxy]hexyl]oxy]-, 4-Methoxyphenyl ester
• CAS NO: 82200-53-1
• Molecular Formula: C₂₃H₂₆O₆
• Molecular Weight: 398.44894
• Mol File: 82200-53-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 539.9±45.0 °C(Predicted)
• Appearance: /
• Density: 1.133±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester(82200-53-1)
• EPA Substance Registry System: Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester(82200-53-1)

Safety Data

• Hazardous Substances Data: 82200-53-1(Hazardous Substances Data)

Usage

General Description

"Benzoesure, 4-[[6-[(1-oxo-2-propenyl)oxy]hexyl]oxy]-, 4-methoxyphenylester is a complex chemical compound whose name indicates its multi-component structure. It contains parts of benzoic acid (Benzoesure), propenyl (1-oxo-2-propenyl), hexyl (a six-carbon chain), and methoxyphenyl ester. The "oxy" and "ester" components suggest oxygen-containing groups attached to the base molecules. The exact properties of this compound, including its potential uses, reactivity, toxicity, and pharmacological effects, would depend on the exact arrangement and bonding of these components. Such information would require a more detailed chemical analysis or research studies on this specific compound.

Upstream product

• 150-76-5 4-methoxy-phenol 
• 83883-26-5 4-{[6-(acryloyloxy)hexyl]oxy}benzoic acid 
• 83883-25-4 4-(6-hydroxyhexyloxy)benzoic acid 
• 4286-55-9 1-bromo-6-hexanol 
• 99-96-7 4-hydroxy-benzoic acid 

Relevant articles and documents

Allyl sulfide-based visible light-induced dynamically reshaped liquid crystalline elastomer/SWCNT nanocomposites capable of multimode NIR photomechanical actuations

Liquid crystalline elastomers (LCEs) combine the ordering character of a liquid crystal and the elasticity of a polymer network. The development of fully light-driven LCE-based soft actuators with good reshapeability and recyclability is in high demand. In this work, we prepared SWCNT/LCE composite films through the introduction of allyl sulfide-based dynamic covalent crosslinks in the LCE matrix and the well-dispersed filler single-walled carbon nanotubes (SWCNTs) with a strong photothermal effect. The SWCNT/LCE composite films were facilely fabricated with reorientation and remouldable capabilities regulated by 405 nm visible light. The monodomain composite films demonstrated multimode actuations of contraction, bending, curling, stretching recovery, and even shape memory driven by 808 nm near-infrared (NIR) light. Moreover, the monodomain spiral ribbon or stretching flat strip and the original polydomain composite film can be readily transformed into each other, and reshaped through easily achievable fabrication conditions. Therefore, the well-prepared SWCNT/LCE composite films with exchangeable covalent crosslinks showed promise as candidates for the development of multimode NIR photomechanical soft actuators with fully light-driven controllability and good remouldability. This journal is